反应 #4135634
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-4cf607409e79428a874b813e2302093f暂无可渲染的结构数据
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2-(甲氨基)环己-1-醇(CAS 92344-45-1)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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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4cf607409e79428a874b813e2302093f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-07a73a5287314e6aa9d57b7837fa9320反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1c9edf7d50bd46fcb289296b142c0395反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7e009cbc5f334649bc5db51e386d7ef2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4cf607409e79428a874b813e2302093f反应条件: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of (2-hydroxy-cyclohexyl)-carbamic acid ethyl ester (2.06 g, 11.0 mmol, 1.0 eq.) in THF (80 mL) was added LiAlH4 (1.09 g, 28.7 mmol, 2.6 eq.) and the resulting mixture was heated at 65° C. for 2 h. The reaction mixture was cooled to 0° C., quenched with water, and the separated aqueous phase was extracted with 3×EtOAc. The combined organic phase was dried over MgSO4, filtered and concentrated to give 2-methylamino-cyclohexanol (1.19 g, 84%). The reaction mixture was cooled to 0° C. quenched with water the separated aqueous phase was extracted with 3×EtOAc The combined organic phase was dried over MgSO4 filtered concentrated
来源 ID: ord-c31a0b1e22ff43f7a338c88071aa01db反应条件: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of (2-hydroxy-cyclohexyl)-carbamic acid ethyl ester (2.06 g, 11.0 mmol, 1.0 eq.) in THF (80 mL) was added LiAlH4 (1.09 g, 28.7 mmol, 2.6 eq.) and the resulting mixture was heated at 65° C. for 2 h. The reaction mixture was cooled to 0° C., quenched with water, and the separated aqueous phase was extracted with 3×EtOAc. The combined organic phase was dried over MgSO4, filtered and concentrated to give 2-methylamino-cyclohexanol (1.19 g, 84%). The reaction mixture was cooled to 0° C. quenched with water the separated aqueous phase was extracted with 3×EtOAc The combined organic phase was dried over MgSO4 filtered concentrated
来源 ID: ord-c31a0b1e22ff43f7a338c88071aa01db反应条件: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of (2-hydroxy-cyclohexyl)-carbamic acid ethyl ester (2.06 g, 11.0 mmol, 1.0 eq.) in THF (80 mL) was added LiAlH4 (1.09 g, 28.7 mmol, 2.6 eq.) and the resulting mixture was heated at 65° C. for 2 h. The reaction mixture was cooled to 0° C., quenched with water, and the separated aqueous phase was extracted with 3×EtOAc. The combined organic phase was dried over MgSO4, filtered and concentrated to give 2-methylamino-cyclohexanol (1.19 g, 84%). The reaction mixture was cooled to 0° C. quenched with water the separated aqueous phase was extracted with 3×EtOAc The combined organic phase was dried over MgSO4 filtered concentrated
来源 ID: ord-c31a0b1e22ff43f7a338c88071aa01db反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-07a73a5287314e6aa9d57b7837fa9320反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1c9edf7d50bd46fcb289296b142c0395反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7e009cbc5f334649bc5db51e386d7ef2反应条件: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of (2-hydroxy-cyclohexyl)-carbamic acid ethyl ester (2.06 g, 11.0 mmol, 1.0 eq.) in THF (80 mL) was added LiAlH4 (1.09 g, 28.7 mmol, 2.6 eq.) and the resulting mixture was heated at 65° C. for 2 h. The reaction mixture was cooled to 0° C., quenched with water, and the separated aqueous phase was extracted with 3×EtOAc. The combined organic phase was dried over MgSO4, filtered and concentrated to give 2-methylamino-cyclohexanol (1.19 g, 84%). The reaction mixture was cooled to 0° C. quenched with water the separated aqueous phase was extracted with 3×EtOAc The combined organic phase was dried over MgSO4 filtered concentrated
来源 ID: ord-ee435313d2df42daaa0add3299571340PubChem 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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