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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243642Generated: October 27, 2026

Benzyl chloroformate → Ethyl(3-{[(benzyloxy)carbonyl]amino}phenyl)acetate

https://huagongshe.com/reaction/243642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 3-aminophenylacetateHCID 13054266—
SolventDichloromethaneHCID 6344—
ProductEthyl(3-{[(benzyloxy)carbonyl]amino}phenyl)acetateHCID 57907493—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl (3-aminophenyl)acetate (25 g, 140 mmol) in 250 mL anhydrous DCM was added DIEA (28.5 mL, 155 mmol) and the resulting solution cooled to 0° C. and set under nitrogen atmosphere. To this cooled solution was then added benzyl chloroformate (21.1 mL, 148 mmol) and the resulting mixture stirred overnight allowing to warm to room temperature. The reaction was washed with 1 M HCl, water, and then brine. The organic layer was dried over sodium sulfate, filtered and concentrated under vacuum. No further purification was necessary and the material (44 g, 99%) was used as is for the next step reaction. LC-MS: m/z (ES) 314 (MH)+, 336 (MNa)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653260B2
Source datasetuspto-grants-2014_02
ORD IDord-99c5c4fb42c34c63ba28b8078c31b16d
Source noteuspto-grants-2014_02