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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82436Generated: October 26, 2026

Methyl bromoacetate → Oleyl bromoacetate

https://huagongshe.com/reaction/82436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl bromoacetateHCID 60984—
ReactantOleyl AlcoholHCID 5284499—
ProductOleyl bromoacetateHCID 56640678—

Reaction Steps

Technical grade oleyl alcohol (85 wt %; 10 g; 37.2 mmol) was combined with Novozym 435 (200 mg) in an amber bottle. Methyl bromoacetate (6.84 g; 44.7 mmol; 1.2 equiv.) was added, and the mixture was sealed and stirred at room temperature overnight to afford about 50% conversion to oleyl bromoacetate. The mixture was then purged with a subsurface stream of nitrogen 2.5 days to afford 98.5% conversion of oleyl alcohol to oleyl bromoacetate according to GC analysis. The mixture was filtered, and the solid was washed with toluene. The filtrate was concentrated to give the desired product as a viscous colorless oil (13.19 g, 91%). The product was used in the subsequent reactions without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846723B2
Source datasetuspto-grants-2014_09
ORD IDord-7b981f4a1b054da2a604a68cfd4aad30
Source noteuspto-grants-2014_09