反応 #4110446
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-2b1675941aae43c492cd69d62837d84b表示可能な構造データがありません
C1=CC=C(C=C1)COC(=O)CCBr製品情報
benzyl 3-bromopropanoate (CAS 90841-55-7) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 252570
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
11 反応 · 11 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-2b1675941aae43c492cd69d62837d84b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-c7e51193a5394d8895bd4e787eef79d9反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-5edae4ec4bd14cbe8efe05929f404402反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-c7e51193a5394d8895bd4e787eef79d9反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-5edae4ec4bd14cbe8efe05929f404402反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-2b1675941aae43c492cd69d62837d84b反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-fa166e0ebb5c4a788fedb68a6dd51e86反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-dd7871717cb541f39511b4fa59cf04a5反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-a0d92048bc0c403ebf5ce361383b9599反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-c7e51193a5394d8895bd4e787eef79d9反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-5edae4ec4bd14cbe8efe05929f404402PubChem References
化合物の公開データベース記録に掲載された情報源です。
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