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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743658Generated: November 4, 2026

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

https://huagongshe.com/reaction/1743658

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 numberUS07012071B2
Source datasetuspto-grants-2006_03
ORD IDord-94acc30ae5c54ffeb65c0801da320dec
Source noteuspto-grants-2006_03