HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434513Generated: October 28, 2026
4-Toluenesulfonyl chloride → HCID 13189269, compound
https://huagongshe.com/reaction/434513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | HCID 13189266 | HCID 13189266 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 13189269 | HCID 13189269 | — |
Reaction Steps
A mixture of 2.37 g (0.0033 mol) of [1α,3β]-1,3-bis[(tetrahydro-2H-pyran-2-yl)oxy]-25-(1-ethoxyethoxy)-24,24-difluorocholest-5-en-21-ol, 7 mL of pyridine and 1.27 g (0.0067 mol) of p-toluenesulfonyl chloride was stirred at 0° C. for 18 hr. The mixture was quenched with ice chips. The mixture was then poured into water and extracted with methylene chloride. The organic phase was washed with 10% aqueous sulfuric acid and saturated aqueous sodium bicarbonate solution. The organic layer was dried over anhydrous magnesium sulfate, filtered and evaporated to dryness to yield oily [1α,3β]-1,3-bis[(tetrahydro-2H-pyran-2-yl)oxy]-25-(1-ethoxyethoxy)-24,24-difluorocholest-5-en-21-ol 21-(4-methylbenzenesulfonate), [α]D20 +6° (c 1, CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04397847 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-e8ea24638c9a405da111ceb40e084735 |
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| Source note | uspto-grants-1983_08 |
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