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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198158Generated: October 31, 2026

Sodium methanesulfonate → 1-(2-Methanesulfonyl-thiazol-5-yl)-propan-1-one

https://huagongshe.com/reaction/2198158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanesulfonateHCID 638112—
Reactant1-(2-Bromothiazol-5-yl)propan-1-oneHCID 59278085—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Product1-(2-Methanesulfonyl-thiazol-5-yl)-propan-1-oneHCID 59278397—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 1-(2-bromo-thiazol-5-yl)-propan-1-one (75 mg, 0.34 mmol) in dimethyl sulfoxide (3 mL) was added the sodium methanesulfonate (41 mg, 0.34 mmol) followed by copper (I) iodide (65 mg, 0.34 mmol). The mixture was heated in a microwave at 120° C. for 1 hour. The reaction was diluted with EtOAc (20 mL) and washed with saturated aqueous sodium bicarbonate solution (50 mL) and brine (10 mL). The aqueous phase was extracted with EtOAc (2×10 mL). The combined organic extracts were dried over magnesium sulfate, filtered and concentrated to afford 1-(2-methanesulfonyl-thiazol-5-yl)-propan-1-one which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338610B2
Source datasetuspto-grants-2012_12
ORD IDord-58db530ecfdb4440bec72f07f32eb801
Source noteuspto-grants-2012_12