反応 #4069389
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9348acc7d3f6410b857195f669a9c716表示可能な構造データがありません
C1COC(=O)N1CCC2=CC=C(C=C2)N製品情報
3-[2-(4-aminophenyl)ethyl]-1,3-oxazolidin-2-one (CAS 777834-73-8) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 10703476
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9348acc7d3f6410b857195f669a9c716反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Sodium sulphate (78.3 g) is added to a solution of trichloroacetaldehyde hydrate (32.5 mmoles) in water (100 ml). To the resulting suspension there are added a solution of 3-[2-(4-amino-phenyl)ethyl]oxazolidin-2-one in water (20 ml) and concentrated HCl solution (2.83 ml). A solution of hydroxylamine hydrochloride (95 mmoles) in water (50 ml) is then added. The reaction mixture is heated at reflux for two hours. The mixture is then cooled to ambient temperature. The solid formed is then filtered off, washed with water and dried in vacuo in the presence of P2O5 and at 40° C. overnight to yield the title product, which is used directly in the next Step. The reaction mixture is heated at reflux for two hours The solid formed is then filtered off washed with water dried in vacuo in the presence of P2O5 and at 40° C. overnight
ソース ID: ord-64e59fa5f1e24f38bf1b501021197d01反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Sodium sulphate (78.3 g) is added to a solution of trichloroacetaldehyde hydrate (32.5 mmoles) in water (100 ml). To the resulting suspension there are added a solution of 3-[2-(4-amino-phenyl)ethyl]oxazolidin-2-one in water (20 ml) and concentrated HCl solution (2.83 ml). A solution of hydroxylamine hydrochloride (95 mmoles) in water (50 ml) is then added. The reaction mixture is heated at reflux for two hours. The mixture is then cooled to ambient temperature. The solid formed is then filtered off, washed with water and dried in vacuo in the presence of P2O5 and at 40° C. overnight to yield the title product, which is used directly in the next Step. The reaction mixture is heated at reflux for two hours The solid formed is then filtered off washed with water dried in vacuo in the presence of P2O5 and at 40° C. overnight
ソース ID: ord-64e59fa5f1e24f38bf1b501021197d01反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Pd/C 10% (500 mg) is added to a solution of the compound obtained in Step B (16.6 mmoles) in MeOH (100 ml). The reaction mixture is stirred at 50° C. under 4.5 bars of hydrogen for 4 hours. The catalyst is filtered off and then washed with MeOH. The filtrate is evaporated to dryness and the product obtained is triturated in 10 ml of MeOH. The solid obtained is filtered off and dried in vacuo at 40° C. overnight to yield the title product in the form of a white solid, which is used directly in the next Step. The catalyst is filtered off washed with MeOH The filtrate is evaporated to dryness the product obtained is triturated in 10 ml of MeOH The solid obtained is filtered off dried in vacuo at 40° C. overnight
ソース ID: ord-2da470e3f7c74a7fb72a30e9026f1529反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Pd/C 10% (500 mg) is added to a solution of the compound obtained in Step B (16.6 mmoles) in MeOH (100 ml). The reaction mixture is stirred at 50° C. under 4.5 bars of hydrogen for 4 hours. The catalyst is filtered off and then washed with MeOH. The filtrate is evaporated to dryness and the product obtained is triturated in 10 ml of MeOH. The solid obtained is filtered off and dried in vacuo at 40° C. overnight to yield the title product in the form of a white solid, which is used directly in the next Step. The catalyst is filtered off washed with MeOH The filtrate is evaporated to dryness the product obtained is triturated in 10 ml of MeOH The solid obtained is filtered off dried in vacuo at 40° C. overnight
ソース ID: ord-2da470e3f7c74a7fb72a30e9026f1529反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Pd/C 10% (500 mg) is added to a solution of the compound obtained in Step B (16.6 mmoles) in MeOH (100 ml). The reaction mixture is stirred at 50° C. under 4.5 bars of hydrogen for 4 hours. The catalyst is filtered off and then washed with MeOH. The filtrate is evaporated to dryness and the product obtained is triturated in 10 ml of MeOH. The solid obtained is filtered off and dried in vacuo at 40° C. overnight to yield the title product in the form of a white solid, which is used directly in the next Step. The catalyst is filtered off washed with MeOH The filtrate is evaporated to dryness the product obtained is triturated in 10 ml of MeOH The solid obtained is filtered off dried in vacuo at 40° C. overnight
ソース ID: ord-154339485dc2458b9a183fae320e5d75反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Pd/C 10% (500 mg) is added to a solution of the compound obtained in Step B (16.6 mmoles) in MeOH (100 ml). The reaction mixture is stirred at 50° C. under 4.5 bars of hydrogen for 4 hours. The catalyst is filtered off and then washed with MeOH. The filtrate is evaporated to dryness and the product obtained is triturated in 10 ml of MeOH. The solid obtained is filtered off and dried in vacuo at 40° C. overnight to yield the title product in the form of a white solid, which is used directly in the next Step. The catalyst is filtered off washed with MeOH The filtrate is evaporated to dryness the product obtained is triturated in 10 ml of MeOH The solid obtained is filtered off dried in vacuo at 40° C. overnight
ソース ID: ord-154339485dc2458b9a183fae320e5d75反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Sodium sulphate (78.3 g) is added to a solution of trichloroacetaldehyde hydrate (32.5 mmoles) in water (100 ml). To the resulting suspension there are added a solution of 3-[2-(4-amino-phenyl)ethyl]oxazolidin-2-one in water (20 ml) and concentrated HCl solution (2.83 ml). A solution of hydroxylamine hydrochloride (95 mmoles) in water (50 ml) is then added. The reaction mixture is heated at reflux for two hours. The mixture is then cooled to ambient temperature. The solid formed is then filtered off, washed with water and dried in vacuo in the presence of P2O5 and at 40° C. overnight to yield the title product, which is used directly in the next Step. The reaction mixture is heated at reflux for two hours The solid formed is then filtered off washed with water dried in vacuo in the presence of P2O5 and at 40° C. overnight
ソース ID: ord-64e59fa5f1e24f38bf1b501021197d01反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Pd/C 10% (500 mg) is added to a solution of the compound obtained in Step B (16.6 mmoles) in MeOH (100 ml). The reaction mixture is stirred at 50° C. under 4.5 bars of hydrogen for 4 hours. The catalyst is filtered off and then washed with MeOH. The filtrate is evaporated to dryness and the product obtained is triturated in 10 ml of MeOH. The solid obtained is filtered off and dried in vacuo at 40° C. overnight to yield the title product in the form of a white solid, which is used directly in the next Step. The catalyst is filtered off washed with MeOH The filtrate is evaporated to dryness the product obtained is triturated in 10 ml of MeOH The solid obtained is filtered off dried in vacuo at 40° C. overnight
ソース ID: ord-2da470e3f7c74a7fb72a30e9026f1529反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Sodium sulphate (78.3 g) is added to a solution of trichloroacetaldehyde hydrate (32.5 mmoles) in water (100 ml). To the resulting suspension there are added a solution of 3-[2-(4-amino-phenyl)ethyl]oxazolidin-2-one in water (20 ml) and concentrated HCl solution (2.83 ml). A solution of hydroxylamine hydrochloride (95 mmoles) in water (50 ml) is then added. The reaction mixture is heated at reflux for two hours. The mixture is then cooled to ambient temperature. The solid formed is then filtered off, washed with water and dried in vacuo in the presence of P2O5 and at 40° C. overnight to yield the title product, which is used directly in the next Step. The reaction mixture is heated at reflux for two hours The solid formed is then filtered off washed with water dried in vacuo in the presence of P2O5 and at 40° C. overnight
ソース ID: ord-487f88ec2cbf40ff8accf80c7ce6dbb9反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Pd/C 10% (500 mg) is added to a solution of the compound obtained in Step B (16.6 mmoles) in MeOH (100 ml). The reaction mixture is stirred at 50° C. under 4.5 bars of hydrogen for 4 hours. The catalyst is filtered off and then washed with MeOH. The filtrate is evaporated to dryness and the product obtained is triturated in 10 ml of MeOH. The solid obtained is filtered off and dried in vacuo at 40° C. overnight to yield the title product in the form of a white solid, which is used directly in the next Step. The catalyst is filtered off washed with MeOH The filtrate is evaporated to dryness the product obtained is triturated in 10 ml of MeOH The solid obtained is filtered off dried in vacuo at 40° C. overnight
ソース ID: ord-3b9be956c013464f9262d597b2d2fc5d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9348acc7d3f6410b857195f669a9c716PubChem References
化合物の公開データベース記録に掲載された情報源です。
関連製品
12 related records
CAS 109853-53-4
CAS 139264-67-8
CAS 152305-23-2
CAS 1492825-59-8
CAS 54357-62-9
CAS 41936-95-2
CAS 144222-20-8
CAS 444588-24-3
CAS 1019443-34-5
CAS 917824-18-1
CAS 1002726-96-6
CAS 916421-36-8
見積依頼
仕様、数量、納入先、用途をご連絡ください。供給可否を確認します。
