HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439946Generated: November 1, 2026
Methanesulfonyl chloride → HCID 10711497, compound
https://huagongshe.com/reaction/1439946
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 10562764 | HCID 10562764 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 10711497 | HCID 10711497 | — |
Reaction Steps
The alcohol described in (b) above (12.6 mg) was dissolved in dichloromethane (2.5 ml) and triethylamine (0.07 ml). This solution was cooled to 0° C. Methanesulfonyl chloride (0.04 ml) was added to the solution dropwise. After stirring for 10 mins the solution was diluted with water and the organic layer was separated, dried (MgSO4), filtered and the solvent removed in vacuo to yield a white solid which was used in the following reaction without further purification. 1H NMR (250 MHz, CDCl3) d 2.44 (3H, s, ArH), 2.94 (3H, s, SO2CH3), 5.51 (2H, s, CH2SO2), 7.08 (1H, d, J=1.5 Hz, imidazole-H), 7.40 (2H, d, J=8.0 Hz, ArH), 7.49 (1H, d, J=1.5 Hz, imidazole-H), 7.92 (2H, d, J=8.0 Hz, ArH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05496833 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-ff061d22d944442f80d18606b652b08c |
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| Source note | uspto-grants-1996_03 |
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