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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179148Generated: October 31, 2026

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

https://huagongshe.com/reaction/1179148

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 numberUS07279472B2
Source datasetuspto-grants-2007_10
ORD IDord-9427b2e96f8946b0ab334e35864a3978
Source noteuspto-grants-2007_10