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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584607Generated: October 29, 2026

Epichlorohydrin → HCID 22313555, compound

https://huagongshe.com/reaction/584607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22313664HCID 22313664—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 22313555HCID 223135555%

Reaction Steps

A solution of methyl 2-[(2-hydroxybenzoyl)amino]-2-methylpropanoate, K2CO3 (20 mmol, 2.68 g) and 2-(chloromethyl)oxirane (22 mmol, 2.03 g) in acetonitrile (60 ml) was stirred at reflux temperature overnight. The reaction mixture was diluted with EtOAc and washed with 1.8% HCl/aq (250 ml) and sat. NaCl/aq (250 ml). The organic phase was dried over Na2SO4 and concentrated at reduced pressure. The residue was purified on C18-column (H2O:CH3CN, 0.1M NH4OAc buffer, gradient 10% to 95% CH3CN) to give the subtitle compound (244 mg, 5% yield, two steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06927222B2
Source datasetuspto-grants-2005_08
ORD IDord-89a0650f4c314785a44134c85ad54c59
Source noteuspto-grants-2005_08