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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891584Generated: October 30, 2026

Potassium ethanethioate → HCID 69543961, compound

https://huagongshe.com/reaction/891584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium ethanethioateHCID 23670855—
Reactant(3R)-1-(4-ethoxycarbonyl-1,3-thiazol-2-yl)-3-methanesulfonyloxypyrrolidineHCID 86590855—
SolventDimethylformamideHCID 6228—
ProductHCID 69543961HCID 69543961104.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of (3R)-1-(4-ethoxycarbonyl-1,3-thiazol-2-yl)-3-methanesulfonyloxypyrrolidine (1.0 g, 3.12 mmol) (obtained as described in Reference Example 20(1)) in dimethylformamide (30 ml) was added potassium thioacetate (919 mg, 9.36 mmol) at room temperature. The mixture was stirred in an oil bath (80° C.) for 5.5 hours. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and 10% aqueous sodium chloride solution. The organic layer was washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using toluene:acetonitrile (3:1→1:1) as the eluant to afford (3S)-3-acetyl-1-(4-ethoxycarbonyl-1,3-thiazol-2-yl)pyrrolidine (877 mg, yield 99%) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-c249f17fea27447fb210dcc1dd91a506
Source noteuspto-grants-2006_02