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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559693Generated: October 29, 2026

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

https://huagongshe.com/reaction/559693

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 numberUS08063065B2
Source datasetuspto-grants-2011_11
ORD IDord-0642320d8446462b95f4acc89f7bc0bc
Source noteuspto-grants-2011_11