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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47322Generated: October 29, 2026

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

https://huagongshe.com/reaction/47322

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 numberUS06699870B2
Source datasetuspto-grants-2004_03
ORD IDord-11aed2d71e964a3bbac8429b05982f37
Source noteuspto-grants-2004_03