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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434513Generated: October 28, 2026

4-Toluenesulfonyl chloride → HCID 13189269, compound

https://huagongshe.com/reaction/434513

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 13189266HCID 13189266—
SolventPyridineHCID 1049—
ProductHCID 13189269HCID 13189269—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04397847
Source datasetuspto-grants-1983_08
ORD IDord-e8ea24638c9a405da111ceb40e084735
Source noteuspto-grants-1983_08