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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300158Generated: November 1, 2026

Ammonium Chloride → Tert-butyl 4-allyl-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/2300158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantHCID 178455850HCID 178455850—
SolventDiethyl EtherHCID 3283—
ProductTert-butyl 4-allyl-4-hydroxypiperidine-1-carboxylateHCID 21955339—

Reaction Steps

800 ml solution of 25.0 g tert-butyl 4-oxo-1-piperidinecarboxylate in diethyl ether was cooled in ice/methanol, and 138 ml solution of allylmagnesium bromide (1 M in diethyl ether) was added dropwise thereinto. The reaction mixture was stirred for 3 hr and 10 min. The reaction solution was poured into a mixture of saturated aqueous ammonium chloride and ice. The diethyl ether layer was recovered and washed with brine. It was dried over anhydrous magnesium sulfate, and then filtered. The filtrate was evaporated, and the resulting residue was purified by silica gel column chromatography to give 15.9 g of tert-butyl 4-allyl-4-hydroxy-1-piperidinecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498159B1
Source datasetuspto-grants-2002_12
ORD IDord-816f92eb136e46d8a6b612c3eb22be3e
Source noteuspto-grants-2002_12