Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471206Generated: October 30, 2026

Potassium Cyanide → tert-Butyl 4-(cyanomethyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/471206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactanttert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 22135564—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-(cyanomethyl)-4-hydroxypiperidine-1-carboxylateHCID 25067313—

Reaction Steps

A solution of tert-butyl 1-oxa-6-azaspiro[2.5]octane-6-carboxylate (2 g) in DMF (20 mL) was treated with potassium cyanide (0.672 g) and the resultant mixture stirred at 20° C. for 4 days. The mixture was partitioned between ethyl acetate and brine, the organic layer was washed twice with brine, dried over sodium sulphate, filtered and the solvent evaporated under reduced pressure. The crude product was purified by flash silica chromatography using 60% ethyl acetate in isohexane as solvent. Pure fractions were evaporated to dryness to afford the subtitled compound. Yield 1.18 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629271B2
Source datasetuspto-grants-2014_01
ORD IDord-5fac47384f2a471f9c9bab619a6addd5
Source noteuspto-grants-2014_01