Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069754Generated: October 28, 2026

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

https://huagongshe.com/reaction/1069754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantHCID 178462451HCID 178462451—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-ethynyl-4-hydroxypiperidine-1-carboxylateHCID 18366117—

Reaction Steps

A solution of ethynylmagnesium chloride in THF (100 mL, 50 mmol) was diluted with THF (50 mL) and cooled in an ice—water bath. A solution of Boc-4-piperidone (5.06 g, 25.4 mmol) (Aldrich) in THF (50 mL) was added dropwise over 15 min. The mixture was stirred with cooling for 3 h. Aqueous ammonium chloride solution (100 mL, 15% W/V) was then added and the resulting mixture extracted with ether (2×200 mL). The ether layers were washed with saturated aqueous sodium chloride solution (200 mL), then combined, dried (MgSO4), filtered and concentrated. The residue was purified by chromatography (Biotage 40M, ethyl acetate—hexanes 1:3, V/V as solvent) to give N-Boc-4-hydroxy-4-ethynyl-piperidine as a colorless oil that solidified on standing. (Yield 5.39 g, 94.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06252086B1
Source datasetuspto-grants-2001_06
ORD IDord-5e67fda0fedb4662ada85ddc51947b0b
Source noteuspto-grants-2001_06