HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665964Generated: November 1, 2026
Methanesulfonyl chloride → HCID 57508922, compound
https://huagongshe.com/reaction/1665964
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 57437436 | HCID 57437436 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57508922 | HCID 57508922 | 88.8% |
Reaction Steps
To a solution of 3-[3-chloro-4-(2-hydroxyethoxy)-5-methoxy-phenyl]-1-(3,5,5-trimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-propan-1-one (160 mg, 0.40 mmol) in DCM (10 mL) and DIPEA (0.11 mL, 0.64 mmol) is added methane sulfonylchloride (0.04 mL, 0.48 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-chloro-6-methoxy-4-[3-oxo-3-(3,5,5-trimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-propyl]-phenoxy}-ethyl ester (183 mg) as a yellow oil; LC-MS: tR=1.15 min, [M+1]+=515.15.
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-f12e3cb5edfc4e95bcb357dfc52c7f13 |
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| Source note | uspto-grants-2011_10 |
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