Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491269Generated: October 26, 2026

2-Chlorothiazole → 1-(2-Chlorothiazol-5-yl)ethanone

https://huagongshe.com/reaction/491269

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorothiazoleHCID 76429—
ReactantN-Methoxy-N-methylacetamideHCID 537505—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Chlorothiazol-5-yl)ethanoneHCID 5177731173%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-chlorothiazole (2.5 g, 21 mmol) in THF (10 mL) was added dropwise to a chilled (−75° C.) 2.5 M hexanes solution of n-BuLi (9.2 mL, 23 mmol) in THF (70 mL). After the addition was complete the reaction mixture was stirred for 1 hr. Then a solution of N-methoxy-N-methylacetamide (2.4 g, 23 mmol) in THF (5 mL) was added. The reaction was allowed to stir overnight while warming to 25° C. The reaction was diluted with H2O and thrice extracted with ethyl ether. The organic portions were combined, washed with brine and then dried (Na2SO4). Filtration and removal of solvent gave a residue that was purified by flash chromatography on silica eluting with 5 percent Et2O in pentane, affording product as a white solid, 2.5 g, 15.5 mmol, 73 percent yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531482B2
Source datasetuspto-grants-2009_05
ORD IDord-3e95e4c4c79240cb8344f791c8b89da2
Source noteuspto-grants-2009_05