反应 #4057384
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-bacda8839a5b4fcd8c89dca6b99c8562暂无可渲染的结构数据
CCOC(=O)CCC1=CC(=C(C=C1)Br)O产品信息
乙基 3-(4-溴-3-羟基苯基)丙酸甲酯(CAS 702687-44-3)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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11 条反应 · 11 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-bacda8839a5b4fcd8c89dca6b99c8562反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a −10° C. solution of 3-(3-hydroxy-phenyl)-propionic acid ethyl ester (2.0 g, 10.31 mmol) in chloroform (0.2 M, 51 mL) was added N-bromosuccinimide (1.93 g, 10.83 mmol). After stirring at RT overnight, the solution was concentrated in vacuo and purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes) to give the product as a colorless oil (0.45 g, 16%). the solution was concentrated in vacuo purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes)
来源 ID: ord-8f701f9309fd4b62bbd3569b2ee19397反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a −10° C. solution of 3-(3-hydroxy-phenyl)-propionic acid ethyl ester (2.0 g, 10.31 mmol) in chloroform (0.2 M, 51 mL) was added N-bromosuccinimide (1.93 g, 10.83 mmol). After stirring at RT overnight, the solution was concentrated in vacuo and purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes) to give the product as a colorless oil (0.45 g, 16%). the solution was concentrated in vacuo purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes)
来源 ID: ord-8f701f9309fd4b62bbd3569b2ee19397反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a −10° C. solution of 3-(3-hydroxy-phenyl)-propionic acid ethyl ester (2.0 g, 10.31 mmol) in chloroform (0.2 M, 51 mL) was added N-bromosuccinimide (1.93 g, 10.83 mmol). After stirring at RT overnight, the solution was concentrated in vacuo and purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes) to give the product as a colorless oil (0.45 g, 16%). the solution was concentrated in vacuo purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes)
来源 ID: ord-cc04f682fdd0450685eac8a69a26e2d5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-bacda8839a5b4fcd8c89dca6b99c8562反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a −10° C. solution of 3-(3-hydroxy-phenyl)-propionic acid ethyl ester (2.0 g, 10.31 mmol) in chloroform (0.2 M, 51 mL) was added N-bromosuccinimide (1.93 g, 10.83 mmol). After stirring at RT overnight, the solution was concentrated in vacuo and purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes) to give the product as a colorless oil (0.45 g, 16%). the solution was concentrated in vacuo purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes)
来源 ID: ord-e279e149b6fe4cc1ba4a79efd1e5e2be反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a −10° C. solution of 3-(3-hydroxy-phenyl)-propionic acid ethyl ester (2.0 g, 10.31 mmol) in chloroform (0.2 M, 51 mL) was added N-bromosuccinimide (1.93 g, 10.83 mmol). After stirring at RT overnight, the solution was concentrated in vacuo and purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes) to give the product as a colorless oil (0.45 g, 16%). the solution was concentrated in vacuo purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes)
来源 ID: ord-f0d5ac09597b4d6ca5b9c78acbcbeecc反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a −10° C. solution of 3-(3-hydroxy-phenyl)-propionic acid ethyl ester (2.0 g, 10.31 mmol) in chloroform (0.2 M, 51 mL) was added N-bromosuccinimide (1.93 g, 10.83 mmol). After stirring at RT overnight, the solution was concentrated in vacuo and purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes) to give the product as a colorless oil (0.45 g, 16%). the solution was concentrated in vacuo purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes)
来源 ID: ord-976ce7b0f4ee4f0ab3fe7078de343abd反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a −10° C. solution of 3-(3-hydroxy-phenyl)-propionic acid ethyl ester (2.0 g, 10.31 mmol) in chloroform (0.2 M, 51 mL) was added N-bromosuccinimide (1.93 g, 10.83 mmol). After stirring at RT overnight, the solution was concentrated in vacuo and purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes) to give the product as a colorless oil (0.45 g, 16%). the solution was concentrated in vacuo purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes)
来源 ID: ord-3409da99364c4933b8061224701dda77反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a −10° C. solution of 3-(3-hydroxy-phenyl)-propionic acid ethyl ester (2.0 g, 10.31 mmol) in chloroform (0.2 M, 51 mL) was added N-bromosuccinimide (1.93 g, 10.83 mmol). After stirring at RT overnight, the solution was concentrated in vacuo and purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes) to give the product as a colorless oil (0.45 g, 16%). the solution was concentrated in vacuo purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes)
来源 ID: ord-8f701f9309fd4b62bbd3569b2ee19397反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a −10° C. solution of 3-(3-hydroxy-phenyl)-propionic acid ethyl ester (2.0 g, 10.31 mmol) in chloroform (0.2 M, 51 mL) was added N-bromosuccinimide (1.93 g, 10.83 mmol). After stirring at RT overnight, the solution was concentrated in vacuo and purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes) to give the product as a colorless oil (0.45 g, 16%). the solution was concentrated in vacuo purified by flash column chromatography (SiO2, 5% to 15% ethyl acetate/hexanes)
来源 ID: ord-cc04f682fdd0450685eac8a69a26e2d5PubChem References
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