HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053967Generated: October 30, 2026
Methanesulfonyl chloride → HCID 86730300, compound
https://huagongshe.com/reaction/1053967
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 86730301 | HCID 86730301 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86730300 | HCID 86730300 | — |
Reaction Steps
A solution of 4-hydroxytetrahydrothiophene-3-carbonitrile (1.0 g, 7.7 mmol) in DCM (15 mL) was stirred at 0° C. TEA (4.3 mL, 31 mmol) was added followed by the dropwise addition of methanesulfonyl chloride (1.77 g, 15.5 mmol). The resulting mixture was stirred at 0° C. for 30 minutes then warmed to ambient temperature and stirred for an additional 30 minutes. The mixture was carefully diluted with water and extracted with DCM (2×). The combined organic extracts were washed with 1N aqueous HCl, brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The crude residue was purified by MPLC on silica gel (using a gradient elution of 0-5% MeOH/DCM) to afford the title compound, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394282B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-6b6f60c240584a4fa845607064e75263 |
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| Source note | uspto-grants-2016_07 |
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