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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744061Generated: October 30, 2026

3-Bromophenol → Methyl 2-(3-bromophenoxy)-4-methylpentanoate

https://huagongshe.com/reaction/1744061

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromophenolHCID 11563—
ReactantMethyl 2-bromo-4-methylpentanoateHCID 12957039—
ReactantPotassium tert-butoxideHCID 23665647—
SolventBicarbonate IonHCID 769—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(3-bromophenoxy)-4-methylpentanoateHCID 22235997—

Reaction Steps

3-Bromophenol (2.99 g, 17 mmoles) in a mixture of DMF (3 mL) and THF (15 mL) was treated with potassium tert-butoxide (1.85 g, 16.5 mmoles) and stirred for 30 minutes. Methyl 2-bromo-4-methylpentanoate (2.5 mL, 15.75 mmoles) was added in one portion and the reaction was stirred overnight. The reaction was diluted with diethyl ether, water and sat. aq. bicarbonate. The phases were separated and the organic phase was washed with 2 portions of 1.2 N hydrochloric acid and then brine. The organic phase was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to afford a residue which was purified by flash chromatography to give methyl 2-(3-bromophenoxy)-4-methylpentanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07012075B2
Source datasetuspto-grants-2006_03
ORD IDord-501cb777237344d1be28d3a2c737cee8
Source noteuspto-grants-2006_03