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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542669Generated: October 26, 2026

Hydroquinone → 2-(Benzylsulfanyl)ethyl 2-(4-hydroxyphenoxy)propanoate

https://huagongshe.com/reaction/542669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroquinoneHCID 785—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Benzylsulfanyl)ethyl 2-bromopropanoateHCID 13309630—
SolventDimethylformamideHCID 6228—
Product2-(Benzylsulfanyl)ethyl 2-(4-hydroxyphenoxy)propanoateHCID 13309629—

Reaction Steps

12.1 g of hydroquinone were dissolved in 60 ml of dry dimethylformamide, and while blowing a slow stream of nitrogen into the solution, 31.7 g of potassium carbonate were added thereto at room temperature whilst stirring. Then the mixture was heated to 90° to 95° C. for one hour with stirring. The mixture was cooled to 60° C., and 30.3 g of 2-benzylthioethyl 2-bromopropionate were added dropwise thereto. After the addition was completed, the mixture was further heated to 90° C. for 2 hours. After cooling the reaction mixture to room temperature, it was poured into ice-water and adjusted to pH 7. Then it was extracted with 100 ml of chloroform. The organic phase was dried and the chloroform was distilled off under reduced pressure. The end product of 2-benzylthioethyl 2-(4-hydroxy-phenoxy)-propionate was obtained in a yield of 25.2 g in the form of a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659370
Source datasetuspto-grants-1987_04
ORD IDord-2661097d4b224866bb3b939c7a97d7aa
Source noteuspto-grants-1987_04