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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36228Generated: October 25, 2026

Methanol → Methyl 2-bromo-3-methylbutanoate

https://huagongshe.com/reaction/36228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-Bromoisovaleric acidHCID 11268—
ProductMethyl 2-bromo-3-methylbutanoateHCID 228837—

Reaction Steps

2-Bromo-3-methylbutyric acid (3.65 g, 20 mmole) was esterified in refluxing methanol containing 2 mL concentrated sulfuric acid for 22 hours. After cooling to room temperature, volatiles were evaporated and the residue was taken up in 50 mL of water and extracted with Et2O. The ether layer was washed with 5% aq. NaHCO3, water brine, and dried over Na2SO4. The desired material was obtained after filtration and removal of volatiles; homogeneous by TLC in 4/1 hexane/EtOAc.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411980
Source datasetuspto-grants-1995_05
ORD IDord-98c0c321d20e4334998dacb0a35817c2
Source noteuspto-grants-1995_05