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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503713Generated: October 25, 2026

Water → 2-((2-Chloro-4-nitrophenoxy)methyl)thiazole

https://huagongshe.com/reaction/503713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-1-fluoro-4-nitrobenzeneHCID 67688—
Reactant1,3-Thiazol-2-ylmethanolHCID 2795213—
SolventDimethylformamideHCID 6228—
Product2-((2-Chloro-4-nitrophenoxy)methyl)thiazoleHCID 5340100699.2%

Reaction Steps

2-(2-Chloro-4-nitro-phenoxymethyl)-thiazole is prepared by adding thiazol-2-yl-methanol (2.74 g, 23.76 mmol) to a slurry of sodium hydride (1.21 g of a 60% dispersion in oil, 30.2 mmol) in DMF (10 ml) at 0° C. After several minutes, 2-chloro-1-fluoro-4-nitro-benzene (3.79 g, 21.60 mmol) is added and the reaction mixture warmed to room temperature. The reaction mixture is stirred at room temperature for 3 h, and 60° C. for 16 h. After cooling to room temperature, the reaction mixture is poured into 200 ml water. The resulting precipitate is collected by filtration, washed with water, and dried in vacuo to give 2-(2-chloro-4-nitro-phenoxymethyl)-thiazole (5.80 g, 99%) which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07777032B2
Source datasetuspto-grants-2010_08
ORD IDord-67f5b023283a446ba94788242228c1aa
Source noteuspto-grants-2010_08