反応 #4116221
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-c283622f07d74fbda4c9f09a398c0d2f表示可能な構造データがありません
C1=CC(=C(C=C1Br)N)CO製品情報
(2-amino-4-bromophenyl)methanol (CAS 946122-05-0) 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 53440895
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
9 反応 · 9 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-c283622f07d74fbda4c9f09a398c0d2f反応条件: temp:75.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of (4-bromo-2-nitro-phenyl)-methanol (1.85 g, 7.97 mmol), iron powder (2.23 g, 39.9 mmol), ammonium chloride (213 mg, 3.99 mmol), ethanol (20 mL), and water (10 mL) was heated at 75° C. for 1 h, then after cooling filtered through a pad of diatomaceous earth. The filtrate was evaporated and the residue partitioned between ethyl acetate and water, the organic layer was washed with brine, dried (MgSO4), and evaporated to produce (2-amino-4-bromo-phenyl)-methanol (1.53 g, 90%). Off-white solid, MS (EI)=201.0 (M+). after cooling filtered through a pad of diatomaceous earth The filtrate was evaporated the residue partitioned between ethyl acetate and water the organic layer was washed with brine dried (MgSO4) evaporated
ソース ID: ord-fd49680148b04e8eadaabd019223b480反応条件: temp:75.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of (4-bromo-2-nitro-phenyl)-methanol (1.85 g, 7.97 mmol), iron powder (2.23 g, 39.9 mmol), ammonium chloride (213 mg, 3.99 mmol), ethanol (20 mL), and water (10 mL) was heated at 75° C. for 1 h, then after cooling filtered through a pad of diatomaceous earth. The filtrate was evaporated and the residue partitioned between ethyl acetate and water, the organic layer was washed with brine, dried (MgSO4), and evaporated to produce (2-amino-4-bromo-phenyl)-methanol (1.53 g, 90%). Off-white solid, MS (EI)=201.0 (M+). after cooling filtered through a pad of diatomaceous earth The filtrate was evaporated the residue partitioned between ethyl acetate and water the organic layer was washed with brine dried (MgSO4) evaporated
ソース ID: ord-fd49680148b04e8eadaabd019223b480反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-c283622f07d74fbda4c9f09a398c0d2f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of (2-amino-4-bromo-phenyl)-methanol (1.53 g, 7.57 mmol) in pyridine (15 mL) was treated with 5-chloro-2-methoxybenzenesulfonyl chloride (1.85 g, 7.57 mmol) at room temperature and stirred for 72 h, then poured upon ice-cold 2 M aq. hydrochloric acid solution and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4), and evaporated to produce a gummy residue, from which the product was precipitated by addition of toluene. The precipitate was collected by filtration and dried to afford N-(5-bromo-2-hydroxymethyl-phenyl)-5-chloro-2-methoxy-benzenesulfonamide (2.51 g, 82%). Off-white solid, MS (ISP)=404.2 (M−H)−. extracted with ethyl acetate The organic layer was washed with brine dried (MgSO4) evaporated to produce a gummy residue from which the product was precipitated by addition of toluene The precipitate was collected by filtration dried
ソース ID: ord-8ecfda0949a747b7897e65f00a34f470反応条件: temp:75.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of (4-bromo-2-nitro-phenyl)-methanol (1.85 g, 7.97 mmol), iron powder (2.23 g, 39.9 mmol), ammonium chloride (213 mg, 3.99 mmol), ethanol (20 mL), and water (10 mL) was heated at 75° C. for 1 h, then after cooling filtered through a pad of diatomaceous earth. The filtrate was evaporated and the residue partitioned between ethyl acetate and water, the organic layer was washed with brine, dried (MgSO4), and evaporated to produce (2-amino-4-bromophenyl)-methanol (1.53 g, 90%). Off-white solid, MS (EI)=201.0 (M+). after cooling filtered through a pad of diatomaceous earth The filtrate was evaporated the residue partitioned between ethyl acetate and water the organic layer was washed with brine dried (MgSO4) evaporated
ソース ID: ord-08611a73a7db4a3fb2c2f74ef3e60cc9反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of (2-amino-4-bromo-phenyl)-methanol (1.53 g, 7.57 mmol) in pyridine (15 mL) was treated with 5-chloro-2-methoxybenzenesulfonyl chloride (1.85 g, 7.57 mmol) at room temperature and stirred for 72 h, then poured upon ice-cold 2 M aq. hydrochloric acid solution and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4), and evaporated to produce a gummy residue, from which the product was precipitated by addition of toluene. The precipitate was collected by filtration and dried to afford N-(5-bromo-2-hydroxymethyl-phenyl)-5-chloro-2-methoxy-benzenesulfonamide (2.51 g, 82%). Off-white solid, MS (ISP)=404.2 (M−H)−. extracted with ethyl acetate The organic layer was washed with brine dried (MgSO4) evaporated to produce a gummy residue from which the product was precipitated by addition of toluene The precipitate was collected by filtration dried
ソース ID: ord-d71509574d20457099894d504f9f341d反応条件: temp:75.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of (4-bromo-2-nitro-phenyl)-methanol (1.85 g, 7.97 mmol), iron powder (2.23 g, 39.9 mmol), ammonium chloride (213 mg, 3.99 mmol), ethanol (20 mL), and water (10 mL) was heated at 75° C. for 1 h, then after cooling filtered through a pad of diatomaceous earth. The filtrate was evaporated and the residue partitioned between ethyl acetate and water, the organic layer was washed with brine, dried (MgSO4), and evaporated to produce (2-amino-4-bromo-phenyl)-methanol (1.53 g, 90%). Off-white solid, MS (EI)=201.0 (M+). after cooling filtered through a pad of diatomaceous earth The filtrate was evaporated the residue partitioned between ethyl acetate and water the organic layer was washed with brine dried (MgSO4) evaporated
ソース ID: ord-750b8360f5894fb8a77b7e6101fc8346反応条件: temp:75.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A mixture of (4-bromo-2-nitro-phenyl)-methanol (1.85 g, 7.97 mmol), iron powder (2.23 g, 39.9 mmol), ammonium chloride (213 mg, 3.99 mmol), ethanol (20 mL), and water (10 mL) was heated at 75° C. for 1 h, then after cooling filtered through a pad of diatomaceous earth. The filtrate was evaporated and the residue partitioned between ethyl acetate and water, the organic layer was washed with brine, dried (MgSO4), and evaporated to produce (2-amino-4-bromo-phenyl)-methanol (1.53 g, 90%). Off-white solid, MS (EI)=201.0 (M+). after cooling filtered through a pad of diatomaceous earth The filtrate was evaporated the residue partitioned between ethyl acetate and water the organic layer was washed with brine dried (MgSO4) evaporated
ソース ID: ord-fd49680148b04e8eadaabd019223b480PubChem 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。
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