Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202340Generated: November 1, 2026

Allyl bromide → Tert-butyl 4-allyl-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/2202340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-allyl-4-hydroxypiperidine-1-carboxylateHCID 21955339—

Reaction Steps

To a solution of tert-butyl 4-oxopiperidine-1-carboxylate (10 g, 50.2 mmol), allyl bromide (10.8 mL, 124 mmol) in THF (10 mL), and saturated ammonium chloride solution (50 mL) was added Zn dust (6.5 g, 100 mmol) portionwise below 10° C. After addition was complete, the reaction mixture was stirred overnight, when TLC indicated consumption of s.m. The reaction mixture was diluted with water (50 mL) and acidified with several drops of 10% H2SO4 to pH=6. The reaction mixture was extracted with EtOAc (3×200 mL). The organic layers were combined and washed with a saturated solution of NaHCO3, brine and evaporated, to give the crude product which was purified by chromatography to give title compound 11B as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365545B2
Source datasetuspto-grants-2016_06
ORD IDord-8137ed892ce849ea8f8a22eb48be07e0
Source noteuspto-grants-2016_06