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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231719Generated: October 26, 2026

Pyridine → 1-Methanesulfonyloxy-2,2,5,5-tetramethylcyclopentane

https://huagongshe.com/reaction/231719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant2,2,5,5-Tetramethylcyclopentan-1-olHCID 551696—
SolventDichloromethaneHCID 6344—
Product1-Methanesulfonyloxy-2,2,5,5-tetramethylcyclopentaneHCID 1378237528.6%

Reaction Steps

2.84 g of 2,2,5,5-tetramethylcyclopentanol and 3.2 ml of pyridine were dissolved in 20 ml of methylene chloride, and 4.5 g of methanesulfonyl chloride was added thereto. The mixture was stirred at room temperature for 12 hours, and then 50 ml of aqueous saturated sodium hydrogen carbonate solution was added thereto. The mixture was extracted with 50 ml of ethyl acetate, and the organic layer was washed with aqueous 10% copper sulfate solution, and concentrated under reduced pressure. The resulting residue was recrystallized from n-hexane, whereby 1.26 g of 1-methanesulfonyloxy-2,2,5,5-tetramethylcyclopentane was obtained (m.p. 46° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04847390
Source datasetuspto-grants-1989_07
ORD IDord-6c09d014ffb9417a824fddb49fd9c689
Source noteuspto-grants-1989_07