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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14477Generated: October 29, 2026

Benzyl Alcohol → [8-Bromo-3-(4-chlorophenyl)-2-isopropyl-4-oxo-4H-chromen-7-yl]carbamic acid benzyl ester

https://huagongshe.com/reaction/14477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantPhosgeneHCID 6371—
ReactantTriethylamineHCID 8471—
Reactant7-Amino-8-bromo-3-(4-chlorophenyl)-2-isopropyl-chromen-4-oneHCID 59724244—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product[8-Bromo-3-(4-chlorophenyl)-2-isopropyl-4-oxo-4H-chromen-7-yl]carbamic acid benzyl esterHCID 68701803—

Reaction Steps

A stirred solution of 7-amino-8-bromo-3-(4-chlorophenyl)-2-isopropyl-chromen-4-one (0.242 g, 0.62 mmol) in anhydrous methylene chloride (5 ml) is treated with a 20% solution of phosgene in toluene (0.5 ml). After 3 h, triethylamine (0.12 g, 0.17 ml, 1.24 mmol, 2 eq.) is added, followed by benzyl alcohol (0.067 g, 0.064 ml, 0.62 mmol), and the solution is stirred at room temperature overnight. The solution is diluted with methylene chloride and washed with water. The organic layer is dried (magnesium sulfate) and filtered, and the solvent is removed by evaporation in vacuo. The resulting solid is purified by flash chromatography (cyclohexane/ethyl acetate=9:1) to afford the title compound as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732435B2
Source datasetuspto-grants-2010_06
ORD IDord-398268ad58a94c6b93819e262fefdffd
Source noteuspto-grants-2010_06