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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648929Generated: October 31, 2026

Benzyl chloroformate → Benzyl 4-chloro-5-cyano-2,3,6,7-tetrahydro-1H-azepine-1-carboxylate

https://huagongshe.com/reaction/1648929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
Reactant1-Benzyl-4-chloro-5-cyano-2,3,6,7-tetrahydro-1H-azepineHCID 13072032—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-chloro-5-cyano-2,3,6,7-tetrahydro-1H-azepine-1-carboxylateHCID 13072036—

Reaction Steps

4.3 gm=3.9 ml (0.025 mol) of benzyl chloroformate dissolved in 15 ml of methylene chloride, were added dropwise to a solution of 4.9 gm (0.02 mol) of 1-benzyl-4-chloro-5-cyano-2,3,6,7-tetrahydro-1H-azepine in 500 ml of methylene chloride while stirring at room temperature, whereby the temperature rose by 5° C. The mixture was stirred for 5 hours at room temperature and then allowed to stand overnight. The solvent was then removed in a rotary evaporator, and the residue was purified on a silicagel column (toluene/ethyl acetate=8:2). After the corresponding fractions had been concentrated by evaporation, a slightly yellowish oil was obtained with solidified upon standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04414225
Source datasetuspto-grants-1983_11
ORD IDord-9ee8245e49ec4a498c0416aea38e1629
Source noteuspto-grants-1983_11