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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093347Generated: October 31, 2026

Ethyl chloroformate → Ethyl (3-hydroxymethylphenyl)carbamate

https://huagongshe.com/reaction/2093347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Aminobenzyl alcoholHCID 80293—
SolventDichloromethaneHCID 6344—
ProductEthyl (3-hydroxymethylphenyl)carbamateHCID 10607893—

Reaction Steps

50 g (406 mmol) of 3-aminobenzyl alcohol are suspended in 750 ml of dichloromethane under a nitrogen atmosphere and stirred at room temperature for 30 min and subsequently cooled to 0° C. 49 g (452 mmol) of ethyl chloroformate are slowly added dropwise. After the addition, the reaction mixture is stirred for 20 h and at the same time slowly warmed to room temperature. 300 ml of 1M potassium carbonate solution are added to the suspension formed (evolution of gas!). The organic phase is separated off, the aqueous phase is extracted with 200 ml of dichloromethane, the combined organic phases are washed with saturated sodium chloride solution, dried over sodium sulfate, and the solvent is distilled off.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445489B2
Source datasetuspto-grants-2013_05
ORD IDord-e0c4354332b04c9380855daefa0313b5
Source noteuspto-grants-2013_05