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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3335Generated: October 25, 2026

Dichloromethane → N-(6-Cyanohexanoyl)glycine, ethyl ester

https://huagongshe.com/reaction/3335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CyanideHCID 9032—
ReactantN-(6-bromohexanoyl)-glycine, ethyl esterHCID 86154941—
SolventEthanolHCID 702—
ProductN-(6-Cyanohexanoyl)glycine, ethyl esterHCID 8570769099%

Reaction Steps

23.73 g (84.7·10-3 mol) of N-(6-bromohexanoyl)-glycine, ethyl ester are dissolved in 200 ml of ethanol, and 6.5 g (0.1 mol) of powdered potassium cyanide are added. The reaction mixture is brought to the reflux point and stirred under reflux for 15 hours. After concentration of the mixture under reduced pressure, the residue is taken up with dichloromethane and the organic phase is washed with aqueous sodium chloride solution. The organic phase is dried and concentrated under reduced pressure to give 19 g of the expected product (yield=99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05733928
Source datasetuspto-grants-1998_03
ORD IDord-f0e0f1638dcd40c780aa7d8ec6375945
Source noteuspto-grants-1998_03