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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423038Generated: October 26, 2026

Ammonium Chloride → 1-(2-Bromo-thiazol-5-yl)-propan-1-ol

https://huagongshe.com/reaction/1423038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Bromo-1,3-thiazole-5-carbaldehydeHCID 2773259—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(2-Bromo-thiazol-5-yl)-propan-1-olHCID 58443378—

Reaction Steps

To a solution of 2-bromo-thiazole-5-carboxaldehyde (1.00 g, 5.21 mmol) in THF (10 mL) is added a 3 M solution of ethylmagnesium bromide (5.00 mL, 15.0 mmol) in diethyl ether. After 18 hours, the reaction is poured into saturated aqueous ammonium chloride (100 mL) containing crushed ice and diluted with EtOAc (100 mL). The organic phase is separated, washed with saturated aqueous sodium bicarbonate solution (100 mL), dried over sodium sulfate, filtered and concentrated. The compound is purified by silica gel chromatography eluting using a gradient of 0-100% EtOAc in hexanes to provide 1-(2-bromo-thiazol-5-yl)-propan-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927550B2
Source datasetuspto-grants-2015_01
ORD IDord-e00efad969904fcba1d4e343da2d99e2
Source noteuspto-grants-2015_01