反应 #3866977
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-f039c1304be444c19aa52726b0abf9c5暂无可渲染的结构数据
CC(C)(C)OC(=O)NCC1=C(C=C(C=C1)Cl)CO中间体产品
tert-butyl N-[[4-chloro-2-(hydroxymethyl)phenyl]methyl]carbamate
结构、标识符和计算性质已按 CAS 与数据库记录完成匹配。
| 中文名称 | [4-氯-2-(羟基甲基)苄基]氨基甲酸叔丁酯 |
|---|---|
| English name | tert-butyl N-[[4-chloro-2-(hydroxymethyl)phenyl]methyl]carbamate |
| IUPAC 名称 | — |
| CAS号 | 439117-40-5 |
| 数据库编号 | 12052444 |
| 分子式 | — |
| 分子量 | — |
产品信息
[4-氯-2-(羟基甲基)苄基]氨基甲酸叔丁酯(CAS 439117-40-5)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 12052444
安全提示
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合成路线数据
6 条反应 · 6 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f039c1304be444c19aa52726b0abf9c5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tert-butyl 4-chloro-2-(hydroxymethyl)benzylcarbamate (10 g, 36.8 mmol) in anhydrous THF (100 ml) was added DPPA (8.3 ml, 38.6 mmol) and DBU (5.79 ml, 38.6 mmol). The mixture was stirred overnight and then was partitioned between ethyl acetate and water. The organic layer was washed with brine, and was concentrated in vacuo to a crude oil (14.6 g). Purification was accomplished by silica gel chromatography, eluting a gradient of ethyl acetate-hexane (10, 15, 20, 25, 50%) to give tert-butyl 2-(aminomethyl)-4-chlorobenzylcarbamate. was partitioned between ethyl acetate and water The organic layer was washed with brine was concentrated in vacuo to a crude oil (14.6 g) Purification eluting a gradient of ethyl acetate-hexane (10, 15, 20, 25, 50%)
来源 ID: ord-5856e21ad03647968f2456be76a3da00反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tert-butyl 4-chloro-2-(hydroxymethyl)benzylcarbamate (10 g, 36.8 mmol) in anhydrous THF (100 ml) was added DPPA (8.3 ml, 38.6 mmol) and DBU (5.79 ml, 38.6 mmol). The mixture was stirred overnight and then was partitioned between ethyl acetate and water. The organic layer was washed with brine, and was concentrated in vacuo to a crude oil (14.6 g). Purification was accomplished by silica gel chromatography, eluting a gradient of ethyl acetate-hexane (10, 15, 20, 25, 50%) to give tert-butyl 2-(aminomethyl)-4-chlorobenzylcarbamate. was partitioned between ethyl acetate and water The organic layer was washed with brine was concentrated in vacuo to a crude oil (14.6 g) Purification eluting a gradient of ethyl acetate-hexane (10, 15, 20, 25, 50%)
来源 ID: ord-966e639c23184c068a0a97eee6f3ce12反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tert-butyl 4-chloro-2-(hydroxymethyl)benzylcarbamate (10 g, 36.8 mmol) in anhydrous THF (100 ml) was added DPPA (8.3 ml, 38.6 mmol) and DBU (5.79 ml, 38.6 mmol). The mixture was stirred overnight and then was partitioned between ethyl acetate and water. The organic layer was washed with brine, and was concentrated in vacuo to a crude oil (14.6 g). Purification was accomplished by silica gel chromatography, eluting a gradient of ethyl acetate-hexane (10, 15, 20, 25, 50%) to give tert-butyl 2-(aminomethyl)-4-chlorobenzylcarbamate. was partitioned between ethyl acetate and water The organic layer was washed with brine was concentrated in vacuo to a crude oil (14.6 g) Purification eluting a gradient of ethyl acetate-hexane (10, 15, 20, 25, 50%)
来源 ID: ord-5856e21ad03647968f2456be76a3da00反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tert-butyl 4-chloro-2-(hydroxymethyl)benzylcarbamate (10 g, 36.8 mmol) in anhydrous THF (100 ml) was added DPPA (8.3 ml, 38.6 mmol) and DBU (5.79 ml, 38.6 mmol). The mixture was stirred overnight and then was partitioned between ethyl acetate and water. The organic layer was washed with brine, and was concentrated in vacuo to a crude oil (14.6 g). Purification was accomplished by silica gel chromatography, eluting a gradient of ethyl acetate-hexane (10, 15, 20, 25, 50%) to give tert-butyl 2-(aminomethyl)-4-chlorobenzylcarbamate. was partitioned between ethyl acetate and water The organic layer was washed with brine was concentrated in vacuo to a crude oil (14.6 g) Purification eluting a gradient of ethyl acetate-hexane (10, 15, 20, 25, 50%)
来源 ID: ord-966e639c23184c068a0a97eee6f3ce12反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of tert-butyl 4-chloro-2-(hydroxymethyl)benzylcarbamate (10 g, 36.8 mmol) in anhydrous THF (100 ml) was added DPPA (8.3 ml, 38.6 mmol) and DBU (5.79 ml, 38.6 mmol). The mixture was stirred overnight and then was partitioned between ethyl acetate and water. The organic layer was washed with brine, and was concentrated in vacuo to a crude oil (14.6 g). Purification was accomplished by silica gel chromatography, eluting a gradient of ethyl acetate-hexane (10, 15, 20, 25, 50%) to give tert-butyl 2-(aminomethyl)-4-chlorobenzylcarbamate. was partitioned between ethyl acetate and water The organic layer was washed with brine was concentrated in vacuo to a crude oil (14.6 g) Purification eluting a gradient of ethyl acetate-hexane (10, 15, 20, 25, 50%)
来源 ID: ord-5856e21ad03647968f2456be76a3da00PubChem References
以下资料来自该化合物的公开数据库参考记录。
