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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615623Generated: November 1, 2026

Methyl chloroacetate → HCID 13174340, compound

https://huagongshe.com/reaction/1615623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroacetateHCID 7295—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178425983HCID 178425983—
SolventEthanolHCID 702—
ProductHCID 13174340HCID 1317434029%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-aminopyridin-2(1H)-iminium-2,4,6-trimethylbenzenesulfonate (crude product from the previous step) and sodium hydroxide (NaOH) (0.55 g, 13.8 mmol) in EtOH (30 mL) was stirred at 60° C. for 1 h, then methyl 2-chloroacetate (1.12 g, 10.4 mmol) was added. The reaction mixture was refluxed for 4 h, then the solvent was removed. The product was purified by silica gel column chromatography (eluting with 20% v/v EtOAc in PE) to give the title compound (512 mg, yield: 29%, 2 steps). ESI MS: m/z 168 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765760B2
Source datasetuspto-grants-2014_07
ORD IDord-c24ba078bb83499ebfc0ce8da74c7b85
Source noteuspto-grants-2014_07