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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464780Generated: October 30, 2026

Methanesulfonyl chloride → HCID 86747789, compound

https://huagongshe.com/reaction/1464780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 19916949HCID 19916949—
ReactantHCID 19916966HCID 19916966—
ReactantPotassium ethanethioateHCID 23670855—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 86747789HCID 8674778987.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-[3-(3-thienyl)phenyl]ethyl methanesulfonate, [synthesized by reacting 100 mg of 2-[3-(3-thienyl)phenoxy]ethanol with 50 μl of methanesulfonyl chloride and 190 μl of triethylamine in 1 ml of ethyl acetate] was dissolved in 1.5 ml of dimethylformamide, and 68 mg of potassium thioacetate was added. The mixture was heated at 80° C. with stirring for 3 hours, and then water and ethyl acetate were added. The organic layer separated was worked up in a customary manner to give 111 mg of S-[2-[3-(3-thienyl)phenoxy]ethyl] thioacetate as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05306728
Source datasetuspto-grants-1994_04
ORD IDord-bfe78c6d7ab94afc813ac0e89a3f5f42
Source noteuspto-grants-1994_04