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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609985Generated: October 31, 2026

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

https://huagongshe.com/reaction/1609985

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 5321705762.8%

Reaction Steps

A solution of sodium cyanide (1052 mg, 21.5 mmol), ammonium chloride (1265 mg, 23.65 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 numberUS06982272B2
Source datasetuspto-grants-2006_01
ORD IDord-af38690e9a2e48209c5bae9812e009a7
Source noteuspto-grants-2006_01