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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759966Generated: October 24, 2026

Sodium Thiosulfate → 4-(2-Butynyloxy)-6-methanesulfonylpyrimidine

https://huagongshe.com/en/reaction/1759966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-(2-Butynyloxy)-6-methylthiopyrimidineHCID 22599877—
SolventChloroformHCID 6212—
Product4-(2-Butynyloxy)-6-methanesulfonylpyrimidineHCID 22599863—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 14 ml of chloroform were added 4-(2-butynyloxy)-6-methylthiopyrimidine and 3.5 g of m-chloroperbenzoic acid (>65%), followed by stirring at 0° C. for 10 hours. The reaction mixture was then poured into a saturated aqueous sodium thiosulfate solution and extracted three times with chloroform. The chloroform layers were combined, washed with water, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silica gel column chromatography to give 1.4 g of 4-(2-butynyloxy)-6-methanesulfonylpyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838463B2
Source datasetuspto-grants-2005_01
ORD IDord-4fedc6ac9b4648da863d57e9b653d54c
Source noteuspto-grants-2005_01