HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044051Generated: October 27, 2026
Methanesulfonyl chloride → HCID 58556972, compound
https://huagongshe.com/reaction/1044051
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 | HCID 58556972 | HCID 58556972 | — |
Reaction Steps
Ethyl 2-hydroxy-2-(thiophen-2-yl)acetate (I26) (4.58 g, 24.6 mmol) was 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) were added, and the resulting solution was stirred at room temperature for 1 hour. DIPEA (0.86 ml, 4.92 mmol) and methanesulphonyl chloride (0.19 ml, 2.46 mmol) were added again. After 1 additional hour, a third portion of DIPEA (0.43 ml, 2.46 mmol) and methanesulphonyl chloride (77 ul, 0.98 mmol) was added. After 1 hour, the reaction was completed. The mixture was diluted with DCM, washed with sat. NaHCO3, water and brine, dried (Na2SO4), filtered, and evaporated. The resulting oil was used for the next step without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563577B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-8392a2684bb24921b9b4e24feed42829 |
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| Source note | uspto-grants-2013_10 |
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