反应 #4110446
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-2b1675941aae43c492cd69d62837d84b暂无可渲染的结构数据
C1=CC=C(C=C1)COC(=O)CCBr产品信息
苄基3-溴丙酸酯(CAS 90841-55-7)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
11 条反应 · 11 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2b1675941aae43c492cd69d62837d84b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A spatula tip full of p-toluenesulfonic acid monohydrate was added to a solution of 3-bromopropionic acid (20.49 g, 0.134 mol) and benzyl alcohol (15 mL, ~15.7 g, 0.145 mol) in benzene (150 mL). A Dean-Stark trap was fitted to the reaction vessel and the solution was held at reflux with overnight stirring. After 16 hr at reflux, the reaction was cooled, washed with saturated sodium bicarbonate, dried (Na2SO4), and concentrated to an oil (28.78 g). Fractional distillation at reduced pressure (0.18 torr) gave the desired product as a colorless liquid (18.49 g, 56%) boiling in the range 99°-109° C. A Dean-Stark trap was fitted to the reaction vessel at reflux with overnight After 16 hr at reflux the reaction was cooled washed with saturated sodium bicarbonate dried (Na2SO4) concentrated to an oil (28.78 g) Fractional distillation at reduced pressure (0.18 torr)
来源 ID: ord-c7e51193a5394d8895bd4e787eef79d9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A spatula tip full of p-toluenesulfonic acid monohydrate was added to a solution of 3-bromopropionic acid (20.49 g, 0.134 mol) and benzyl alcohol (15 mL, ~ 15.7 g, 0.145 mol) in benzene (150 mL). A Dean-Stark trap was fitted to the reaction vessel and the solution was held at reflux with overnight stirring. After 16 hr at reflux, the reaction was cooled, washed with saturated sodium bicarbonate, dried (Na2SO4), and concentrated to an oil (28.78 g). Fractional distillation at reduced pressure (0.18 torr) gave the desired product as a colorless liquid (18.49 g, 56%) boiling in the range 99°-109° C. A Dean-Stark trap was fitted to the reaction vessel at reflux with overnight After 16 hr at reflux the reaction was cooled washed with saturated sodium bicarbonate dried (Na2SO4) concentrated to an oil (28.78 g) Fractional distillation at reduced pressure (0.18 torr)
来源 ID: ord-5edae4ec4bd14cbe8efe05929f404402反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A spatula tip full of p-toluenesulfonic acid monohydrate was added to a solution of 3-bromopropionic acid (20.49 g, 0.134 mol) and benzyl alcohol (15 mL, ~15.7 g, 0.145 mol) in benzene (150 mL). A Dean-Stark trap was fitted to the reaction vessel and the solution was held at reflux with overnight stirring. After 16 hr at reflux, the reaction was cooled, washed with saturated sodium bicarbonate, dried (Na2SO4), and concentrated to an oil (28.78 g). Fractional distillation at reduced pressure (0.18 torr) gave the desired product as a colorless liquid (18.49 g, 56%) boiling in the range 99°-109° C. A Dean-Stark trap was fitted to the reaction vessel at reflux with overnight After 16 hr at reflux the reaction was cooled washed with saturated sodium bicarbonate dried (Na2SO4) concentrated to an oil (28.78 g) Fractional distillation at reduced pressure (0.18 torr)
来源 ID: ord-c7e51193a5394d8895bd4e787eef79d9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A spatula tip full of p-toluenesulfonic acid monohydrate was added to a solution of 3-bromopropionic acid (20.49 g, 0.134 mol) and benzyl alcohol (15 mL, ~ 15.7 g, 0.145 mol) in benzene (150 mL). A Dean-Stark trap was fitted to the reaction vessel and the solution was held at reflux with overnight stirring. After 16 hr at reflux, the reaction was cooled, washed with saturated sodium bicarbonate, dried (Na2SO4), and concentrated to an oil (28.78 g). Fractional distillation at reduced pressure (0.18 torr) gave the desired product as a colorless liquid (18.49 g, 56%) boiling in the range 99°-109° C. A Dean-Stark trap was fitted to the reaction vessel at reflux with overnight After 16 hr at reflux the reaction was cooled washed with saturated sodium bicarbonate dried (Na2SO4) concentrated to an oil (28.78 g) Fractional distillation at reduced pressure (0.18 torr)
来源 ID: ord-5edae4ec4bd14cbe8efe05929f404402反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2b1675941aae43c492cd69d62837d84b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A spatula tip full of p-toluenesulfonic acid monohydrate was added to a solution of 3-bromopropionic acid (20.49 g, 0.134 mol) and benzyl alcohol (15 mL, ~ 15.7 g, 0.145 mol) in benzene (150 mL). A Dean-Stark trap was fitted to the reaction vessel and the solution was held at reflux with overnight stirring. After 16 hr at reflux, the reaction was cooled, washed with saturated sodium bicarbonate, dried (Na2SO4), and concentrated to an oil (28.78 g). Fractional distillation at reduced pressure (0.18 torr) gave the desired product as a colorless liquid (18.49 g, 56%) boiling in the range 99°-109° C. A Dean-Stark trap was fitted to the reaction vessel at reflux with overnight After 16 hr at reflux the reaction was cooled washed with saturated sodium bicarbonate dried (Na2SO4) concentrated to an oil (28.78 g) Fractional distillation at reduced pressure (0.18 torr)
来源 ID: ord-fa166e0ebb5c4a788fedb68a6dd51e86反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A spatula tip full of p-toluenesulfonic acid monohydrate was added to a solution of 3-bromopropionic acid (20.49 g, 0.134 mol) and benzyl alcohol (15 mL, ~15.7 g, 0.145 mol) in benzene (150 mL). A Dean-Stark trap was fitted to the reaction vessel and the solution was held at reflux with overnight stirring. After 16 hr at reflux, the reaction was cooled, washed with saturated sodium bicarbonate, dried (Na2SO4), and concentrated to an oil (28.78 g). Fractional distillation at reduced pressure (0.18 torr) gave the desired product as a colorless liquid (18.49 g, 56%) boiling in the range 99°-109° C. A Dean-Stark trap was fitted to the reaction vessel at reflux with overnight After 16 hr at reflux the reaction was cooled washed with saturated sodium bicarbonate dried (Na2SO4) concentrated to an oil (28.78 g) Fractional distillation at reduced pressure (0.18 torr)
来源 ID: ord-dd7871717cb541f39511b4fa59cf04a5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A spatula tip full of p-toluenesulfonic acid monohydrate was added to a solution of 3-bromopropionic acid (20.49,g, 0.134 mol) and benzyl alcohol (15 mL, ~ 15.7 g, 0.145 mol) in benzene (150 mL). A Dean-Stark trap was fitted to the reaction vessel and the solution was held at reflux with overnight stirring. After 16 hr at reflux, the reaction was cooled, washed with saturated sodium bicarbonate, dried (Na2SO4), and concentrated to an oil (28.78 g). Fractional distillation at reduced pressure (0.18 torr) gave the desired product as a colorless liquid (18.49 g, 56% ) boiling in the range 99°-109° C. A Dean-Stark trap was fitted to the reaction vessel at reflux with overnight After 16 hr at reflux the reaction was cooled washed with saturated sodium bicarbonate dried (Na2SO4) concentrated to an oil (28.78 g) Fractional distillation at reduced pressure (0.18 torr)
来源 ID: ord-a0d92048bc0c403ebf5ce361383b9599反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A spatula tip full of p-toluenesulfonic acid monohydrate was added to a solution of 3-bromopropionic acid (20.49 g, 0.134 mol) and benzyl alcohol (15 mL, ~15.7 g, 0.145 mol) in benzene (150 mL). A Dean-Stark trap was fitted to the reaction vessel and the solution was held at reflux with overnight stirring. After 16 hr at reflux, the reaction was cooled, washed with saturated sodium bicarbonate, dried (Na2SO4), and concentrated to an oil (28.78 g). Fractional distillation at reduced pressure (0.18 torr) gave the desired product as a colorless liquid (18.49 g, 56%) boiling in the range 99°-109° C. A Dean-Stark trap was fitted to the reaction vessel at reflux with overnight After 16 hr at reflux the reaction was cooled washed with saturated sodium bicarbonate dried (Na2SO4) concentrated to an oil (28.78 g) Fractional distillation at reduced pressure (0.18 torr)
来源 ID: ord-c7e51193a5394d8895bd4e787eef79d9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A spatula tip full of p-toluenesulfonic acid monohydrate was added to a solution of 3-bromopropionic acid (20.49 g, 0.134 mol) and benzyl alcohol (15 mL, ~ 15.7 g, 0.145 mol) in benzene (150 mL). A Dean-Stark trap was fitted to the reaction vessel and the solution was held at reflux with overnight stirring. After 16 hr at reflux, the reaction was cooled, washed with saturated sodium bicarbonate, dried (Na2SO4), and concentrated to an oil (28.78 g). Fractional distillation at reduced pressure (0.18 torr) gave the desired product as a colorless liquid (18.49 g, 56%) boiling in the range 99°-109° C. A Dean-Stark trap was fitted to the reaction vessel at reflux with overnight After 16 hr at reflux the reaction was cooled washed with saturated sodium bicarbonate dried (Na2SO4) concentrated to an oil (28.78 g) Fractional distillation at reduced pressure (0.18 torr)
来源 ID: ord-5edae4ec4bd14cbe8efe05929f404402PubChem 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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