Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826627Generated: November 2, 2026

Methyl chloroformate → HCID 12085579, compound

https://huagongshe.com/reaction/1826627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantTriethylamineHCID 8471—
ReactantHCID 12085578HCID 12085578—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12085579HCID 1208557987.6%

Reaction Steps

To a solution of 4-allyloxy-2′-hydoxybenzophenone (0.87 g) in tetrahydrofuran (14 mL) were added triethylamine (0.53 mL) and methyl chloroformate (0.29 mL) at 0° C., and the mixture was stirred at room temperature for 1.5 hours. An insoluble material was removed by filtration, and the solvent of the filtrate was removed under reduced pressure. To a solution of the residue in tetrahydrofuran (18 mL) and water (9 mL) was added sodium borohydride (0.52 g) at 0° C., and the mixture was stirred at room temperature for 2.5 hours. To the reaction mixture was added 0.5 mol/L aqueous hydrochloric acid solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate=8/1) to give 2-(4-allyloxybenzyl)phenol (0.72 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053060B2
Source datasetuspto-grants-2006_05
ORD IDord-54f24d7e81b34db78d806824cf044569
Source noteuspto-grants-2006_05