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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361191Generated: October 31, 2026

Propanal → 2-Thiazolemethanol, -alpha--ethyl-

https://huagongshe.com/reaction/1361191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanalHCID 527—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-BromothiazoleHCID 76430—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product2-Thiazolemethanol, -alpha--ethyl-HCID 15785702—

Reaction Conditions

Temperature0 °C

Reaction Steps

A 1.3 M solution of i-PrMgCl.LiCl (2.65 mL, 3.44 mmol) under an atmosphere of argon was cooled to −15° C. and treated with a solution of 2-bromothiazole (0.56 g, 3.4 mmol) in anhydrous THF (1 mL). The reaction mixture was then allowed to warm to 0° C. over 15 minutes. Propionaldehyde (0.25 mL, 3.4 mmol) was added and the solution was allowed to warm to room temperature over 18 hours. The solution was poured into saturated aqueous ammonium chloride (50 mL) containing crushed ice. The aqueous layer was extracted with EtOAc (50 mL) and washed with saturated aqueous sodium bicarbonate (100 mL). The aqueous layer was again extracted with EtOAc (50 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated. The material was purified by silica gel chromatography eluting with a gradient of 0-10% methanol in dichloromethane to afford 1-thiazol-2-yl-propan-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879873B2
Source datasetuspto-grants-2011_02
ORD IDord-6483662422804b19a3a1a2611858360d
Source noteuspto-grants-2011_02