Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269178Generated: October 30, 2026

Benzyl Alcohol → Benzyl (5-bromopyridin-3-yl)carbamate

https://huagongshe.com/reaction/1269178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
Reactant5-Bromonicotinic acidHCID 88707—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
SolventTolueneHCID 1140—
ProductBenzyl (5-bromopyridin-3-yl)carbamateHCID 1844684973.2%

Reaction Steps

To a suspension of 5-bromonicotinic acid (20.0 g, 99.0 mmol) in toluene (200 mL) was added diphenylphosphoryl azide (25.6 mL, 118.8 mmol) and Et3N (16.6 mL, 118.8 mmol). After stirring at room temperature for 30 min, benzyl alcohol (15.4 mL, 148.5 mmol) was added. The mixture was stirred at room temperature for 1 h then refluxed overnight. The cold reaction mixture was washed with H2O, NaHCO3 and brine, dried over MgSO4 and concentrated. Purification by flash chromatography (15–50% EtOAc/Hexane) provided 22.2 g (72.5 mmol, 73%) of benzyl 5-bromo-3-pyridinylcarbamate: ESMS m/e: 307.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199135B2
Source datasetuspto-grants-2007_04
ORD IDord-51549b7691c444e3962cb407cfa05dde
Source noteuspto-grants-2007_04