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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1alpha,3beta-Bis(tetrahydropyran-2-yloxy)cholesta-5,7-dien-22-olHCID 22843895—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
Product1alpha,3beta-Bis(tetrahydropyran-2-yloxy)cholesta-5,7-dien-22-yl methanesulfonateHCID 8674583886.7%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359055
Source datasetuspto-grants-1994_10
ORD IDord-916670539c234e6e8e30c1cdd1a35b08
Source noteuspto-grants-1994_10