反応 #4099773
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-a21985412d0d43d3bfe2aa4f58cfa8d8表示可能な構造データがありません
C1CSC2=CC=CC=C2C1O製品情報
3,4-dihydro-2H-thiochromen-4-ol (CAS 40316-60-7) 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 375102
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-a21985412d0d43d3bfe2aa4f58cfa8d8反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Reduction of thiochroman-4-one with lithium aluminum hydride by the method of Preparation O, Part (iii), affords thiochroman-4-ol in like manner. This is taken up in acetic acid containing a molar excess of acetic anhydride, the mixture heated at reflux for three hours, cooled, ethanol added to quench the excess anhydride and the mixture hydrogenated by the method of Example 11.
ソース ID: ord-0ed15ad592464ddb8da349c6de037d0b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Reduction of thiochroman-4-one with lithium aluminum hydride by the method of Preparation O, Part (iii), affords thiochroman-4-ol in like manner. This is taken up in acetic acid containing a molar excess of acetic anhydride, the mixture heated at reflux for three hours, cooled, ethanol added to quench the excess anhydride and the mixture hydrogenated by the method of Example 11.
ソース ID: ord-0ed15ad592464ddb8da349c6de037d0b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of thiochroman-4-one (9 g) in ether (27 ml) was added slowly to a mixture of lithium aluminium hydride (0.53 g) in ether (54 ml). After the end of the addition, the mixture was refluxed for 2 hours. The reaction mixture was cooled and ice was added, followed by water and by a solution of 20% H2SO4. The water phase was washed twice with ether. The ether phase was washed twice with NaOH 2N, and once with water, dried over MgSO4 and evaporated. The clear oil (8.9 g) crystallised after few hours. Rdt=97% After the end of the addition the mixture was refluxed for 2 hours The reaction mixture was cooled ice was added The water phase was washed twice with ether The ether phase was washed twice with NaOH 2N once with water, dried over MgSO4 evaporated The clear oil (8.9 g) crystallised after few hours
ソース ID: ord-f7c18e138d614a18bea372de5f1cb7ca反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of thiochroman-4-one (9 g) in ether (27 ml) was added slowly to a mixture of lithium aluminium hydride (0.53 g) in ether (54 ml). After the end of the addition, the mixture was refluxed for 2 hours. The reaction mixture was cooled and ice was added, followed by water and by a solution of 20% H2SO4. The water phase was washed twice with ether. The ether phase was washed twice with NaOH 2N, and once with water, dried over MgSO4 and evaporated. The clear oil (8.9 g) crystallised after few hours. Rdt=97% After the end of the addition the mixture was refluxed for 2 hours The reaction mixture was cooled ice was added The water phase was washed twice with ether The ether phase was washed twice with NaOH 2N once with water, dried over MgSO4 evaporated The clear oil (8.9 g) crystallised after few hours
ソース ID: ord-8b0ba0af3bdd48759c55ed3cd4e1dbd3反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Reduction of thiochroman-4-one with lithium aluminum hydride by the method of Preparation O, Part (iii), affords thiochroman-4-ol in like manner. This is taken up in acetic acid containing a molar excess of acetic anhydride, the mixture heated at reflux for three hours, cooled, ethanol added to quench the excess anhydride and the mixture hydrogenated by the method of Example 11.
ソース ID: ord-0ed15ad592464ddb8da349c6de037d0b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-a21985412d0d43d3bfe2aa4f58cfa8d8反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of thiochroman-4-one (9 g) in ether (27 ml) was added slowly to a mixture of lithium aluminium hydride (0.53 g) in ether (54 ml). After the end of the addition, the mixture was refluxed for 2 hours. The reaction mixture was cooled and ice was added, followed by water and by a solution of 20% H2SO4. The water phase was washed twice with ether. The ether phase was washed twice with NaOH 2N, and once with water, dried over MgSO4 and evaporated. The clear oil (8.9 g) crystallised after few hours. Rdt=97% After the end of the addition the mixture was refluxed for 2 hours The reaction mixture was cooled ice was added The water phase was washed twice with ether The ether phase was washed twice with NaOH 2N once with water, dried over MgSO4 evaporated The clear oil (8.9 g) crystallised after few hours
ソース ID: ord-678f340c6b884a2d89d27849f85ca94d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of thiochroman-4-one (9 g) in ether (27 ml) was added slowly to a mixture of lithium aluminium hydride (0.53 g) in ether (54 ml). After the end of the addition, the mixture was refluxed for 2 hours. The reaction mixture was cooled and ice was added, followed by water and by a solution of 20% H2SO4. The water phase was washed twice with ether. The ether phase was washed twice with NaOH 2N, and once with water, dried over MgSO4 and evaporated. The clear oil (8.9 g) crystallised after few hours. Rdt=97% After the end of the addition the mixture was refluxed for 2 hours The reaction mixture was cooled ice was added The water phase was washed twice with ether The ether phase was washed twice with NaOH 2N once with water, dried over MgSO4 evaporated The clear oil (8.9 g) crystallised after few hours
ソース ID: ord-a964377c2e80473e97c5c75bcc690004反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of thiochroman-4-one (9 g) in ether (27 ml) was added slowly to a mixture of lithium aluminium hydride (0.53 g) in ether (54 ml). After the end of the addition, the mixture was refluxed for 2 hours. The reaction mixture was cooled and ice was added, followed by water and by a solution of 20% H2SO4. The water phase was washed twice with ether. The ether phase was washed twice with NaOH 2N, and once with water, dried over MgSO4 and evaporated. The clear oil (8.9 g) crystallised after few hours. Rdt=97% After the end of the addition the mixture was refluxed for 2 hours The reaction mixture was cooled ice was added The water phase was washed twice with ether The ether phase was washed twice with NaOH 2N once with water, dried over MgSO4 evaporated The clear oil (8.9 g) crystallised after few hours
ソース ID: ord-f7c18e138d614a18bea372de5f1cb7ca反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of thiochroman-4-one (9 g) in ether (27 ml) was added slowly to a mixture of lithium aluminium hydride (0.53 g) in ether (54 ml). After the end of the addition, the mixture was refluxed for 2 hours. The reaction mixture was cooled and ice was added, followed by water and by a solution of 20% H2SO4. The water phase was washed twice with ether. The ether phase was washed twice with NaOH 2N, and once with water, dried over MgSO4 and evaporated. The clear oil (8.9 g) crystallised after few hours. Rdt=97% After the end of the addition the mixture was refluxed for 2 hours The reaction mixture was cooled ice was added The water phase was washed twice with ether The ether phase was washed twice with NaOH 2N once with water, dried over MgSO4 evaporated The clear oil (8.9 g) crystallised after few hours
ソース ID: ord-8b0ba0af3bdd48759c55ed3cd4e1dbd3反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Reduction of thiochroman-4-one with lithium aluminum hydride by the method of Preparation O, Part (iii), affords thiochroman-4-ol in like manner. This is taken up in acetic acid containing a molar excess of acetic anhydride, the mixture heated at reflux for three hours, cooled, ethanol added to quench the excess anhydride and the mixture hydrogenated by the method of Example 11.
ソース ID: ord-0ed15ad592464ddb8da349c6de037d0bPubChem 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。
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。
