Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811312Generated: November 3, 2026

Ammonia → tert-Butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/1811312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactanttert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 22135564—
SolventEthanolHCID 702—
Producttert-Butyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylateHCID 2339631960.5%

Reaction Steps

A stirred solution of 1-oxa-6-aza-spiro[2.5]octane-6-carboxylic acid tert-butyl ester (9.0 g, 42.2 mmol) in ethanol (60 ml) was added with ammonia (160 ml). The resulting mixture was stirred under a nitrogen atmosphere overnight. The mixture was concentrated under reduced pressure. The residue was added with Water (50 ml) and extracted with ethyl acetate (150 ml×3). The Combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography with dichloromethane:methanol (20:1) as eluents to give 4-aminomethyl-4-hydroxy-piperidine-1-carboxylic acid tert-butyl ester (5.87 g, 60.5%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362251B2
Source datasetuspto-grants-2013_01
ORD IDord-31cd2dd5ce1c41a9baf0222350e6d120
Source noteuspto-grants-2013_01