Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253984Generated: November 2, 2026

3-Pyridineacetic acid → HCID 19746660, compound

https://huagongshe.com/reaction/2253984

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Pyridineacetic acidHCID 108—
ReactantDichloromethaneHCID 6344—
Reactanttert-ButanolHCID 6386—
ReactantBromineHCID 24408—
ReactantPhosphorus pentachlorideHCID 24819—
CatalystPhosphorus tribromideHCID 24614—
SolventPyridineHCID 1049—
ProductHCID 19746660HCID 1974666043.6%

Reaction Steps

After 3.7 ml (71.8 mmols) of bromine and 0.1 ml (0.1 mmol) of phosphorus tribromide were added to 10 g (57.6 mmoles) of 3-pyridylacetic acid, the resulting mixture was stirred at 80° to 90° C. for an hour. At room temperature 150 ml of dichloromethane was added to the mixture and 13.0 g (62.4 mmols) of phosphorus pentachloride was further added thereto. The mixture was stirred for an hour. The solution was dropwise added at -60° to -70° C. to a mixture of 150 ml of dichloromethane, 27 ml of tert-butanol and 23 ml of pyridine. After the temperature was elevated to room temperature, the solution was washed, in sequence, with 1N hydrochloric acid aqueous solution and saturated sodium hydrogencarbonate aqueous solution. The solution was dried over anhydrous magnesium sulfate and the solvent was distilled off. The resulting oil was subjected to silica gel column chromatography and the column was eluted with dichloromethane-methanol (10:1) to give 6.8 g (43.6%) of t-butyl 2-bromo-2-(3-pyridyl)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05233035
Source datasetuspto-grants-1993_08
ORD IDord-3dfc2c6d36b4446799e9612865868201
Source noteuspto-grants-1993_08