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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907042Generated: November 1, 2026

Acetyl chloride → 5-Bromo-2-pyridinyl Acetate

https://huagongshe.com/reaction/907042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 178515818HCID 178515818—
SolventDiethyl EtherHCID 3283—
Product5-Bromo-2-pyridinyl AcetateHCID 2343857652%

Reaction Steps

A suspension of 0.5 g (2.87 mmol) of 5-bromo-2-pyridinol in 10 ml of ethyl ether is prepared and 1 ml (7.1 mmol) of triethylamine and then 1 ml (14 mmol) of acetyl chloride are added at ambient temperature. The mixture is stirred at ambient temperature for 24 hours and then the insoluble materials are removed by filtration. The filtrate is concentrated under reduced pressure and the crude product is purified by chromatography on silica gel, elution being carried out using a toluene/2-propanol mixture (9/1; v/v). The expected product is obtained in the form of a pale yellow powder with a yield of 52%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08013010B2
Source datasetuspto-grants-2011_09
ORD IDord-494fc5c5a5db4fb3a27b111fd16d8f74
Source noteuspto-grants-2011_09