HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464780Generated: October 30, 2026
Methanesulfonyl chloride → HCID 86747789, compound
https://huagongshe.com/reaction/1464780
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 19916949 | HCID 19916949 | — |
| Reactant | HCID 19916966 | HCID 19916966 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86747789 | HCID 86747789 | 87.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05306728 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-bfe78c6d7ab94afc813ac0e89a3f5f42 |
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| Source note | uspto-grants-1994_04 |
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