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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58882Generated: October 28, 2026

Ammonium Chloride → 1-Boc-4-methyl-piperidin-4-OL

https://huagongshe.com/reaction/58882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
Product1-Boc-4-methyl-piperidin-4-OLHCID 2273081292.9%

Reaction Conditions

Temperature-40 °C

Reaction Steps

A solution of N-Boc-piperidin-4-one (1.0 g, 5.0 mmol) was dissolved in THF (20 mL) and then cooled to −40° C. MeMgBr (2.8 M, 7.2 mL, 20 mmol) was added slowly over 10 min. The reaction mixture was allowed to warm to ambient temperature and stirred for 2 h. The mixture was cooled to 0° C. and saturated aqueous NH4Cl (50 mL) was added. The resulting mixture was extracted with EtOAc (100 mL). The organic layer was washed with water (50 mL) and brine (50 mL), dried over anhydrous sodium sulfate, and concentrated to afford tert-butyl 4-hydroxy-4-methylpiperidine-1-carboxylate (1.0 g, 92% yield) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434761B2
Source datasetuspto-grants-2016_09
ORD IDord-332a591d16b646858971d1b293a88d68
Source noteuspto-grants-2016_09