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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228095Generated: October 30, 2026

N-(4-chloromethylphenyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide → N-(4-(cyclohexylthiomethyl)phenyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide

https://huagongshe.com/reaction/2228095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-chloromethylphenyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamideHCID 18472316—
ReactantSodium cyclohexylsulfideHCID 69353652—
SolventDimethylformamideHCID 6228—
ProductN-(4-(cyclohexylthiomethyl)phenyl)-7-(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamideHCID 18472260—

Reaction Steps

A solution of N-(4-chloromethylphenyl)-7—(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide (0.2g) and sodium cyclohexylsulfide (0.08g) in dimethylformamide (10 ml) was stirred at room temperature for 2.5 hours. The solvent was evaporated, and to the residue was added water. The mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated sodium chloride solution, and dried with anhydrous magnesium sulfate. Under reduced pressure, the solvent was evaporated to give crude crystals, which were recrystallized from ethyl acetate-hexane to give N-(4—(cyclohexylthiomethyl)-phenyl)-7—(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide (Compound 53) (0.199) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-106630a60936417b98f9328410c94a4a
Source noteuspto-grants-2002_07