反应 #4116221
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c283622f07d74fbda4c9f09a398c0d2f暂无可渲染的结构数据
C1=CC(=C(C=C1Br)N)CO产品信息
(2-氨基-4-溴苯基)甲醇(CAS 946122-05-0)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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合成路线数据
9 条反应 · 9 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c283622f07d74fbda4c9f09a398c0d2f反应条件: temp:75.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 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
来源 ID: ord-fd49680148b04e8eadaabd019223b480反应条件: temp:75.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 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
来源 ID: ord-fd49680148b04e8eadaabd019223b480反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c283622f07d74fbda4c9f09a398c0d2f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 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
来源 ID: ord-8ecfda0949a747b7897e65f00a34f470反应条件: temp:75.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 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
来源 ID: ord-08611a73a7db4a3fb2c2f74ef3e60cc9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 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
来源 ID: ord-d71509574d20457099894d504f9f341d反应条件: temp:75.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 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
来源 ID: ord-750b8360f5894fb8a77b7e6101fc8346反应条件: temp:75.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 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
来源 ID: ord-fd49680148b04e8eadaabd019223b480PubChem References
以下资料来自该化合物的公开数据库参考记录。
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