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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773963Generated: November 1, 2026

Ethanol → Ethyl 2-(3-bromo-4-hydroxyphenyl)acetate

https://huagongshe.com/reaction/1773963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Bromo-4-hydroxyphenylacetic acidHCID 2769628—
ProductEthyl 2-(3-bromo-4-hydroxyphenyl)acetateHCID 18620106—

Reaction Steps

To a solution of 3-bromo-4-hydroxyphenylacetic acid (1.19 g, 5 mmol, 1 eq.) in EtOH (15 mL), thionyl chloride (0.73 mL, 10 mmol, 2 eq.) was added. The reaction mixture was stirred at r.t. during 1 h 30. The mixture was concentrated in vacuo. The residue was partitioned between DCM (50 mL) and sat. aq. NaHCO3 soln. (50 mL). The layers were separated and the aq. phase was extracted with DCM (2×50 mL). The comb. org. phases were dried over MgSO4, filtered, and concentrated in vacuo to give the title compound as a pale yellow oil. The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255090B2
Source datasetuspto-grants-2016_02
ORD IDord-06de97c5f4c64c2ab21d02c575f825bf
Source noteuspto-grants-2016_02