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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689436Generated: October 31, 2026

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

https://huagongshe.com/reaction/1689436

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 numberUS08148373B2
Source datasetuspto-grants-2012_04
ORD IDord-3d105e8e5454475286e6d718c5cfa143
Source noteuspto-grants-2012_04