HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271385Generated: October 31, 2026
Methanesulfonyl chloride → HCID 72574159, compound
https://huagongshe.com/reaction/271385
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 69275924 | HCID 69275924 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 72574159 | HCID 72574159 | 100% |
Reaction Steps
To a solution of 4-(2-{[tert-Butyl(dimethyl)silyl]oxy}-2-phenylethoxy)-3-fluorocyclohexanol (8.46 g, 22.9 mmol) in dichloromethane (100 mL) at 0° C. was added methanesulfonyl chloride (2.49 mL, 32.1 mmol) and diisopropylethylamine (11.1 mL, 64.1 mmol). The reaction mixture was stirred for 1 min, diluted with dichloromethane and washed with 5% potassium bisulfate. The layers were separated and the aqueous extracted with dichloromethane (3×). The combined organic layers were washed with water and brine, dried over Na2SO4, filtered and concentrated. Purification by flash column chromatography (hexane: ethyl acetate 70:30) gave 4-(2-{[tert-Butyl(dimethyl)silyl]oxy}-2-phenylethoxy)-3-fluorocyclohexyl methanesulfonate (9.77 g, 100% yield) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07452893B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-dd4d3f494d9d4d96b53d35a2665d636f |
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| Source note | uspto-grants-2008_11 |
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