HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261438Generated: November 4, 2026
Methanesulfonyl chloride → HCID 86622506, compound
https://huagongshe.com/reaction/2261438
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 59380606 | HCID 59380606 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86622506 | HCID 86622506 | 98.5% |
Reaction Steps
A solution of 3-[4-(3-hydroxy-propyl)-phenyl]-1-((1aS,5aR)-1,1,2-trimethyl-1,1a,5,5a-tetrahydro-3-thia-cyclopropa[a]pentalen-4-yl)-propan-1-one (147 mg, 0.40 mmol), DIPEA (0.11 mL, 0.642 mmol) in DCM (5 mL) is treated with methane sulfonylchloride (40 μL, 0.481 mmol) at 0° C. The solution is stirred at 0° C. for 30 min, then at rt for 1 h before it is diluted with DCM and washed with 0.1 N aq. NaOH solution, followed by 10% aq. citric acid solution. The organic layer is separated, dried over Na2SO4 and evaporated to give methanesulfonic acid 3-{4-[3-oxo-3-((1aS,5aR)-1,1,2-trimethyl-1,1a,5,5a-tetrahydro-3-thia-cyclopropa[a]pentalen-4-yl)-propyl]-phenyl}-propyl ester (176 mg) as a colourless oil; LC-MS: tR=1.14 min, [M+1]+=447.25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07846964B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-aef171b5a17148268f23680ffedd9c79 |
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| Source note | uspto-grants-2010_12 |
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