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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423070Generated: November 3, 2026

tert-Butanol → HCID 72213060, compound

https://huagongshe.com/reaction/1423070

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant1-(2-Bromopyridin-4-yl)cyclopropane-1-carboxylic acidHCID 71743246—
ProductHCID 72213060HCID 72213060—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of the crude 1-(2-bromopyridin-4-yl)-cyclopropanecarboxylic acid (350 mg, 1.45 mmol) in t-butanol (7 mL) is added diphenylphosphoryl azide (0.312 mL, 1.45 mmol) and triethylamine (0.202 mL, 1.45 mmol) in a pressure vessel. The tube is sealed and the reaction mixture is warmed at 90° C. After 4 hours, the pressure vessel is cooled in an ice-bath, vented and opened. The reaction mixture is concentrated in vacuo. The resulting residue is dissolved in EtOAc (70 mL), washed with saturated aqueous ammonium chloride (70 mL), saturated aqueous sodium bicarbonate (70 mL), dried over MgSO4, filtered and concentrated. The residue is purified by silica gel chromatography eluting with a gradient of 0-50% EtOAc in heptane to afford [1-(2-bromopyridin-4-yl)-cyclopropyl]-carbamic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927550B2
Source datasetuspto-grants-2015_01
ORD IDord-d3b9687bcb8c467785f9422ef35f7b68
Source noteuspto-grants-2015_01