HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665965Generated: October 31, 2026
Methanesulfonyl chloride → HCID 57508923, compound
https://huagongshe.com/reaction/1665965
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 57437437 | HCID 57437437 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57508923 | HCID 57508923 | 97.5% |
Reaction Steps
To a solution of 3-[3-chloro-4-(3-hydroxy-propoxy)-5-methoxy-phenyl]-1-(3,5,5-trimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-propan-1-one (170 mg, 0.38 mmol) in DCM (10 mL) and DIPEA (0.10 mL, 0.60 mmol) is added methane sulfonylchloride (0.04 mL, 0.45 mmol) at 0° C. The reaction mixture is stirred at 0° C. for 30 min. Another portion of methane sulfonylchloride (0.04 mL, 0.45 mmol) is added and stirring is continued for 20 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 3-{2-chloro-6-methoxy-4-[3-oxo-3-(3,5,5-trimethyl-4,5,6,7-tetrahydro-benzo[c]thiophen-1-yl)-propyl]-phenoxy}-propyl ester (196 mg) as a yellow oil; LC-MS: tR=1.17 min, [M+1]+=529.17.
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-a13e6fbf93a04314bdaeda270a098755 |
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| Source note | uspto-grants-2011_10 |
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