Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506587Generated: October 30, 2026

Ammonium Chloride → HCID 67468382, compound

https://huagongshe.com/reaction/1506587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl 4-(4-formyl-1,3-thiazol-2-yl)piperidine-1-carboxylateHCID 7172298—
ReactantHCID 178418865HCID 178418865—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67468382HCID 67468382—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under an argon atmosphere and at −78° C., chloro(2-phenylethyl)magnesium (1M in diethyl ether, 3.77 ml) was added dropwise to a solution of tert-butyl 4-(4-formyl-1,3-thiazol-2-yl)piperidine-1-carboxylate (1.0 g) in tetrahydrofuran (10 ml). The reaction mixture was stirred at −78° C. for one hour, and more chloro(2-phenylethyl)magnesium (3M in diethyl ether, 0.20 ml) was then added dropwise. The reaction mixture was then stirred for 20 minutes. Saturated ammonium chloride solution was then added to the reaction mixture, and the aqueous phase was separated off. After extraction of the aqueous phase with ethyl acetate, the combined organic phases were dried over sodium sulphate and the solvent was removed under reduced pressure. This gave tert-butyl 4-[4-(1-hydroxy-3-phenylpropyl)-1,3-thiazol-2-yl]piperidine-1-carboxylate (790 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09220266B2
Source datasetuspto-grants-2015_12
ORD IDord-4d31ca34264446a4b6c8179dee88bbda
Source noteuspto-grants-2015_12