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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069856Generated: October 30, 2026

Hydrochloric Acid → 4-Bromo-2-(3-hydroxy-1,1,3-trimethyl-butyl)-phenol

https://huagongshe.com/reaction/1069856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
Reactant2H-1-Benzopyran-2-one, 6-bromo-3,4-dihydro-4,4-dimethyl-HCID 22568923—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-Bromo-2-(3-hydroxy-1,1,3-trimethyl-butyl)-phenolHCID 22568810100%

Reaction Steps

A solution of 6-bromo-4,4-dimethyl-chroman-2-one (1 g, 3.92 mmol) in anhydrous tetrahydrofuran (20 mL) was treated with 3M solution of ethyl magnesium bromide (2.6 mL) and stirred at ambient temperature for 2hours. The reaction mixture was poured into cold dilute hydrochloric acid and extracted with ethyl acetate (×2). The combined organic extract was dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to afford a residue which was subjected to flash column chromatography over silica gel (230-400 mesh) using 10% ethyl acetate in hexane as the eluent to afford the title compound as a pale yellow solid (1.1 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06252090B1
Source datasetuspto-grants-2001_06
ORD IDord-563bef108c5040c0821a0f36838b4a7c
Source noteuspto-grants-2001_06