HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665962Generated: October 30, 2026
Methanesulfonyl chloride → HCID 57508920, compound
https://huagongshe.com/reaction/1665962
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 11852049 | HCID 11852049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57508920 | HCID 57508920 | 106.1% |
Reaction Steps
To a solution of 3-[4-(2-hydroxy-ethoxy)-3,5-dimethyl-phenyl]-1-(3,5,5-trimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-propan-1-one (130 mg, 0.325 mmol) in DCM (10 mL) and DIPEA (0.09 mL, 0.52 mmol) is added methane sulfonylchloride (0.03 mL, 0.39 mmol) at 0° C. The reaction mixture is stirred at 0° C. for 30 min. The reaction mixture is diluted with DCM, washed with 0.1 N aq. NaOH followed by 10% aq. citric acid solution, dried over MgSO4 and evaporated to give methanesulfonic acid 2-{2,6-dimethyl-4-[3-oxo-3-(3,5,5-trimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-propyl]-phenoxy}-ethyl ester (165 mg) as a yellow oil; LC-MS: tR=1.17 min, [M+1]+=479.26.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039644B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-80032170218f47b795faade539b68dd1 |
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| Source note | uspto-grants-2011_10 |
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