HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708829Generated: October 31, 2026
Methanesulfonyl chloride → 1alpha,3beta-Bis(tetrahydropyran-2-yloxy)cholesta-5,7-dien-22-yl methanesulfonate
https://huagongshe.com/reaction/1708829
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1alpha,3beta-Bis(tetrahydropyran-2-yloxy)cholesta-5,7-dien-22-ol | HCID 22843895 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1alpha,3beta-Bis(tetrahydropyran-2-yloxy)cholesta-5,7-dien-22-yl methanesulfonate | HCID 86745838 | 86.7% |
Reaction Steps
In 20 ml of pyridine was dissolved 0.58 g of the 1α,3β-bis(tetrahydropyran-2-yloxy)cholesta-5,7-dien-22-ol obtained as above. To this solution was added 0.12 g of methanesulfonyl chloride and the mixture was stirred at 0° C. for 2 hours. Then, at room temperature, the reaction mixture was diluted with water and extracted with diethyl ether. The extract was washed with water and dried over anhydrous sodium sulfate. The low-boiling fraction was then distilled off under reduced pressure and the residue was purified by silica gel column chromatography. The procedure yielded 0.57 g of 1α,3β-bis(tetrahydropyran-2-yloxy)cholesta-5,7-dien-22-yl methanesulfonate (yield: 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05359055 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-916670539c234e6e8e30c1cdd1a35b08 |
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| Source note | uspto-grants-1994_10 |
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