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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742506Generated: November 1, 2026

1-Octanol → Octyl bromoacetate

https://huagongshe.com/reaction/742506

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-OctanolHCID 957—
ReactantPyridineHCID 1049—
ReactantBromoacetyl bromideHCID 61147—
SolventDichloromethaneHCID 6344—
ProductOctyl bromoacetateHCID 34741324.1%

Reaction Steps

Bromoacetyl bromide (20 g, 99.1 mmol) was added to a solution of 1-octanol (12.9 g, 99.1 mmol) and 10 ml of pyridine in 100 ml of methylene chloride at 0° C. After 10 minutes, the mixture was quenched with 100 ml of ice/water, and the aqueous layer was extracted with methylene chloride, and the combined organic layer was washed with 1N HCl (3×100ml) and brine. The organic layer was dried over magnesium sulfate, concentrated in vacuo, and the product was distilled under high vacuum to afford 6 g of 1-octyl bromoacetate as an oil, b.p. 93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554620
Source datasetuspto-grants-1996_09
ORD IDord-c8ec2ea21bf546cfa9c5e03439102de4
Source noteuspto-grants-1996_09