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HRID 450862作成日:2026年10月26日

Ethyl 3-mercaptopropionate → Ethyl 3-((4-hydroxyphenyl)-methylthio)propionate

https://huagongshe.com/reaction/450862

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 3-mercaptopropionateHCID 21625—
反応物Sodium hydrideHCID 24758—
反応物BromocresolHCID 41663—
反応物HCID 178418361HCID 178418361—
溶媒DimethylformamideHCID 6228—
生成物Ethyl 3-((4-hydroxyphenyl)-methylthio)propionateHCID 21964457—

反応手順

To a solution of NaH (60% dispersed in oil, 0.731 g, 21.7 mmol) in dry DMF (15 ml) was added Ethyl 3-mercaptopropionate (2.66 g, 19.8 mmol). When the evolution of hydrogen ceased, 4-Hydroxybenzyl bromide from Step A was added. The reaction mixture was stirred for 16 hours at room temperature, quenched with sat. NH4Cl and concentrated in vacuo. The crude residue was taken in EtOAc and washed with water and brine. The aqueous layer was washed one more time with EtOAc. The combined organic layers were dried over Na2SO4, filtered and concentrated. The purification was done by flash chromatography on silica gel column (dichloromethane:ethyl acetate, 95:5) to provide the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08487000B2
出典データセットuspto-grants-2013_07
ORD IDord-2d581205645746cfa8688cb97c6319ca
出典メモuspto-grants-2013_07