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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274167Generated: November 4, 2026

Thionyl Chloride → 2-Benzyloxy-4-benzyloxycarbonylaminomethylbenzoyl chloride

https://huagongshe.com/reaction/1274167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-Benzyloxy-4-benzyloxycarbonylaminomethylbenzoic acidHCID 22120525—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-Benzyloxy-4-benzyloxycarbonylaminomethylbenzoyl chlorideHCID 22120472—

Reaction Steps

Thionyl chloride (1.55 ml) and dimethylformamide (2 drops) were added to a solution of 2-benzyloxy-4-benzyloxycarbonylaminomethylbenzoic acid (7.1 mg) in dichloromethane (50 ml), and the mixture was refluxed under heating for 1.5 hours. After the reaction, the solvent was evaporated under reduced pressure to give 2-benzyloxy-4-benzyloxycarbonylaminomethylbenzoyl chloride as crystals. Then, the crystals were dissolved in acetonitrile (50 ml), and the solution was dropwise added to a solution of 4-aminopyridine (1.42 g) and diisopropylethylamine (5.27 ml) in acetonitrile (50 ml) under ice-cooling. The mixture was stirred at room temperature for 4 hours. After the reaction, water was added, and the mixture was extracted with chloroform. The extract was washed with water and dried. The solvent was evaporated under reduced pressure, and the obtained crystals were recrystallized from ethyl acetate-hexane to give N-(4-pyridyl)-2-benzyloxy-4-benzyloxycarbonylaminomethylbenzamide as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156766
Source datasetuspto-grants-2000_12
ORD IDord-57f29a0ee9d74e4bb9f12ce9b1b5668e
Source noteuspto-grants-2000_12