Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79318Generated: October 26, 2026

Ethyl formate → Benzyl 2-chloro-3-oxopropanoate

https://huagongshe.com/reaction/79318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl formateHCID 8025—
ReactantAcetic acid, 2-chloro-, phenylmethyl esterHCID 8786—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
ProductBenzyl 2-chloro-3-oxopropanoateHCID 86672210—

Reaction Steps

To potassium tert-butoxide (141 mL, 141 mmol) at 0° C. was added dropwise a solution of benzyl 2-chloroacetate (26.8 g, 141 mmol) and ethyl formate (11.6 mL, 141 mmol) in Et2O (45 mL). The reaction was warmed to ambient temperature and stirred for 16 hours. The reaction mixture was filtered and washed with cold ether (100 mL). The potassium salt was dissolved in H2O (50 mL) and the solution was acidified with concentrated HCl to pH=4 in a cold bath. The solution was extracted with ether and the organic phase was dried (MgSO4) and concentrated to give the crude product. A lower boiling point impurity was removed by vacuum distillation (90° C., 5 mm Hg) and the residue was taken directly to the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841455B2
Source datasetuspto-grants-2014_09
ORD IDord-cd736840933d49b08d4e6330be5fe87d
Source noteuspto-grants-2014_09