Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831805Generated: October 31, 2026

Sodium Hydroxide → tert-Butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/1831805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 23396320HCID 23396320—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylateHCID 23396319—

Reaction Steps

4-Cyano-4-trimethylsilanyloxy-piperidine-1-carboxylic acid tert-butyl ester (7.5 g) was dissolved in 100 ml of tetrahydro-furan under an argon atmosphere. A solution of lithium aluminium hydride in tetrahydro-furan (30 ml, 1 molar) was dropwise added at 0° C. After stirring for 15 hours at room temperature, a sodium hydroxide solution (20%) was slowly added under cooling. The solid was filtered after dilution with ethyl acetate and the organic layer evaporated. The crude material contains a mixture of the desired product (MS: 231.2 (M+H)+) and the corresponding trimethylsiliyl ether (MS: 303.1 (M+H)+) and was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067665B2
Source datasetuspto-grants-2006_06
ORD IDord-5640515c1f784e45bdf80e5bea765115
Source noteuspto-grants-2006_06