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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532839Generated: October 29, 2026

3-(Chloromethyl)pyridine hydrochloride → 4-(3-Pyridylmethoxymethylene)-2-phenylbenzoylmethionine methyl ester

https://huagongshe.com/reaction/1532839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Chloromethyl)pyridine hydrochlorideHCID 23394—
ReactantSodium hydrideHCID 24758—
Reactant[4-Hydroxymethyl-2-phenylbenzoyl]methionine methyl esterHCID 20622833—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-(3-Pyridylmethoxymethylene)-2-phenylbenzoylmethionine methyl esterHCID 67550609—

Reaction Steps

The resultant compound from Example 16D (1.0 equivalent) is treated with sodium hydride (2.0 equivalents) in DMSO, then 3-chloromethylpyridine hydrochloride (1.0 equivalent) is added. When judged complete by TLC analysis, the reaction is diluted with water and ethyl acetate, the organic layer is dried and concentrated, and the crude title compound is purified by chromatography on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06204293B1
Source datasetuspto-grants-2001_03
ORD IDord-b3cb454a506a4f1d9e9fbcceeadadcb9
Source noteuspto-grants-2001_03