反应 #4112019
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-3747a085fd7e4aa0ad6ede3b15ef0ad9暂无可渲染的结构数据
CC(=O)OC1=CC=C(C=C1)CCO中间体产品
[4-(2-hydroxyethyl)phenyl] acetate
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 | Acetic acid 4-(2-hydroxyethyl)phenyl ester |
|---|---|
| English name | [4-(2-hydroxyethyl)phenyl] acetate |
| IUPAC 名称 | — |
| CAS号 | 60037-43-6 |
| 数据库编号 | 586676 |
| 分子式 | — |
| 分子量 | — |
产品信息
Acetic acid 4-(2-hydroxyethyl)phenyl ester(CAS 60037-43-6)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
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数据库编号 586676
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仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
11 条反应 · 11 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3747a085fd7e4aa0ad6ede3b15ef0ad9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0ee1fcd5b7a548139124f4fdfc69b9dc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b55bdac1c9b148aa87aa403109a308d7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A 300 ml Fluitron autoclave (Hastelloy C) is charged with 69.5 g crude acetoxystyrene oxirane (86%; 0.335 mol), 200 ml ethanol and 1.6 g Pd/C (5% Pd on carbon; 47.8% H2O). After sealing, the stirrer is started, and the autoclave purged with nitrogen and hydrogen and then pressurized to 400 psig with hydrogen. The H2 pressure is kept constant during the one hour reaction period. The autoclave is vented and purged with N2. The reaction mixture is sucked out of the reactor (63.2 g ethanol rinse) and filtered (23.7 g ethanol rinse). the autoclave purged with nitrogen and hydrogen The H2 pressure is kept constant during the one hour reaction period purged with N2 The reaction mixture is sucked out of the reactor (63.2 g ethanol rinse) filtered (23.7 g ethanol rinse)
来源 ID: ord-383f67091eb74353b8e2be52883afc64反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A 300 ml Fluitron autoclave (Hastelloy C) is charged with 69.5 g crude acetoxystyrene oxirane (86%; 0.335 mol), 200 ml ethanol and 1.6 g Pd/C (5% Pd on carbon; 47.8% H2O). After sealing, the stirrer is started, and the autoclave purged with nitrogen and hydrogen and then pressurized to 400 psig with hydrogen. The H2 pressure is kept constant during the one hour reaction period. The autoclave is vented and purged with N2. The reaction mixture is sucked out of the reactor (63.2 g ethanol rinse) and filtered (23.7 g ethanol rinse). the autoclave purged with nitrogen and hydrogen The H2 pressure is kept constant during the one hour reaction period purged with N2 The reaction mixture is sucked out of the reactor (63.2 g ethanol rinse) filtered (23.7 g ethanol rinse)
来源 ID: ord-383f67091eb74353b8e2be52883afc64反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3747a085fd7e4aa0ad6ede3b15ef0ad9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0ee1fcd5b7a548139124f4fdfc69b9dc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b55bdac1c9b148aa87aa403109a308d7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 55 g (0.305 mole) 2-(4-methylcarbonyloxyphenyl)-1-ethanol and 34.4 g (0.341 mole) triethylamine in 300 ml dichloromethane were cooled on an ice bath. 38.5 g (0.336 mole) methanesulfonyl chloride was slowly added. The ice bath was removed and the mixture was stirred for 3 hours at room temperature. Water was added and the phases were separated. The organic phase was washed with saturated sodium hydrogen bicarbonate and brine, dried (magnesium sulfate), filtered and evaporated in vacuo to give 76.6 g (yield 97%) of 4-(methylcarbonyloxy)phenethyl methanesulfonate. The ice bath was removed Water was added the phases were separated The organic phase was washed with saturated sodium hydrogen bicarbonate and brine dried (magnesium sulfate) filtered evaporated in vacuo
来源 ID: ord-ebd58084eae847f7b137bb1746131eae反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5.6 g (0.1 mole) potassium hydroxide in 10 ml water was added to a cooled solution of 13.8 g (0.1 mole) p-hydroxyphenethyl alcohol in 50 ml tetrahydrofuran. 10.2 g (0.1 mole) acetic anhydride was slowly added under stirring. After 2 hours diethyl ether and water were added. The phases were separated and the organic phase was dried, filtered and evaporated in vacuo. The product contained 15% starting material and was therefore redissolved in diethyl ether and washed twice with dilute sodium carbonate. Drying, filtration and evaporation of solvents in vacuo gave 12 g (yield 67%) of 2-(4-methylcarbonyloxyphenyl)-1-ethanol which was used without further purification. The phases were separated the organic phase was dried filtered evaporated in vacuo was therefore redissolved in diethyl ether washed twice with dilute sodium carbonate Drying filtration and evaporation of solvents in vacuo
来源 ID: ord-ecd20afd2ef34717a3827cdc48a36da5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A 300 ml Fluitron autoclave (Hastelloy C) is charged with 69.5 g crude acetoxystyrene oxirane (86%; 0.335 mol), 200 ml ethanol and 1.6 g Pd/C (5% Pd on carbon; 47.8% H2O). After sealing, the stirrer is started, and the autoclave purged with nitrogen and hydrogen and then pressurized to 400 psig with hydrogen. The H2 pressure is kept constant during the one hour reaction period. The autoclave is vented and purged with N2. The reaction mixture is sucked out of the reactor (63.2 g ethanol rinse) and filtered (23.7 g ethanol rinse). the autoclave purged with nitrogen and hydrogen The H2 pressure is kept constant during the one hour reaction period purged with N2 The reaction mixture is sucked out of the reactor (63.2 g ethanol rinse) filtered (23.7 g ethanol rinse)
来源 ID: ord-383f67091eb74353b8e2be52883afc64PubChem 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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