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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450862Generated: October 25, 2026

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

https://huagongshe.com/reaction/450862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-mercaptopropionateHCID 21625—
ReactantSodium hydrideHCID 24758—
ReactantBromocresolHCID 41663—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-((4-hydroxyphenyl)-methylthio)propionateHCID 21964457—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08487000B2
Source datasetuspto-grants-2013_07
ORD IDord-2d581205645746cfa8688cb97c6319ca
Source noteuspto-grants-2013_07