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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664794Generated: November 1, 2026

Potassium Cyanide → Benzyl 4-cyano-4-(methylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1664794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
ReactantMethylamine hydrochlorideHCID 6364545—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventMethanol--water (1/1)HCID 22242641—
ProductBenzyl 4-cyano-4-(methylamino)piperidine-1-carboxylateHCID 67440047—

Reaction Steps

A solution of potassium cyanide (2.79 g, 42.9 mmol) in water (5 mL) was added to a solution of benzyl 4-oxopiperidine-1-carboxylate (10.0 g, 42.9 mmol) and methylamine hydrochloride (2.90 g, 42.9 mmol) in water/methanol (1:1; 10 mL) at 0° C. The reaction mixture was allowed to warm to ambient temperature. After 48 h, additional methylamine hydrochloride (1.45 g, 21.4 mmol) was added. After 18 h, the mixture was diluted with ether, and extracted with ethyl acetate (3×). The combined organic extracts were dried over magnesium sulfate and concentrated down to 50 mL volume. HCl gas was bubbled to this solution for 5 min. The solid precipitated out of the solution was filtered and washed with ether (3×), ethyl acetate (3×) and dried under reduced pressure to give the hydrochloride salt of the title compound. MS 274.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039460B2
Source datasetuspto-grants-2011_10
ORD IDord-41754674cd3749fb9cb9f127ffd400a3
Source noteuspto-grants-2011_10