HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255046Generated: October 27, 2026
Methanesulfonyl chloride → Ethyl 2-(methylsulfonyloxy)-2-(thiophen-2-yl)acetate
https://huagongshe.com/reaction/1255046
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 2-hydroxy-2-(thiophen-2-yl)acetate | HCID 12266229 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-(methylsulfonyloxy)-2-(thiophen-2-yl)acetate | HCID 58556972 | — |
Reaction Steps
Hydroxy-thiophen-2-yl-acetic acid ethyl ester (4.58 g, 24.6 mmol) is dissolved in dry DCM (125 mL) and cooled at 0° C. DIPEA (5.15 mL, 29.5 mmol) and methanesulphonyl chloride (2.11 mL, 27.1 mmol) are added and the resulting solution is stirred at RT for 1 hour. DIPEA (0.859 ml, 4.92 mmol) and methanesulphonyl chloride (0.19 mL, 2.46 mmol) are added again. After being stirred at room temperature for 1 additional hour, a third portion of DIPEA (0.43 mL, 2.46 mmol) and methanesulphonyl chloride (77 ul, 0.98 mmol) is added. After 1 hour the reaction is completed. The mixture is diluted with DCM, washed with sat. NaHCO3, water and brine, dried (Na2SO4), filtered and evaporated. The resulting yellow oil is used in the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455646B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-c412baf9c9634e81a981103a7f0ffa3d |
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| Source note | uspto-grants-2013_06 |
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