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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229356Generated: October 30, 2026

Methanol → Benzyl 4-amino-4-cyanopiperidine-1-carboxylate

https://huagongshe.com/reaction/2229356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium CyanideHCID 8929—
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
SolventAmmoniaHCID 222—
ProductBenzyl 4-amino-4-cyanopiperidine-1-carboxylateHCID 53217057369.8%

Reaction Steps

A solution of sodium cyanide (1052 mg, 21.5 mmol), ammonium chloride (1265 mg, 3.65 mmol), and benzyl 4-oxo-1-piperidine-carboxylate (5.0 gm, 21.5 mmol), was prepared in 5 M ammonia in methanol (8.6 mL, 43 mmol). The solution was brought to reflux for 4 h and then allowed to cool to room temperature, The solution was then filtered and washed with methanol (100 mL) and the filtrate was concentrated in vacuo. The resulting oil was taken up in MTBE (250 mL) and filtered again. The filter cake was washed with MTBE (100 mL) and the filtrate was concentrated in vacuo to yield 4-amino-4-cyano-piperidine-1-carboxylic acid benzyl ester as a clear oil (3.5 g) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420364B1
Source datasetuspto-grants-2002_07
ORD IDord-db9142b177bf46f5b230101c3825f2cc
Source noteuspto-grants-2002_07