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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199178Generated: October 29, 2026

Ammonium Chloride → HCID 67468382, compound

https://huagongshe.com/reaction/2199178

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 numberUS09357779B2
Source datasetuspto-grants-2016_06
ORD IDord-183bdfef21284f8c8da1a87aea17569f
Source noteuspto-grants-2016_06