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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892549Generated: October 29, 2026

Methanesulfonyl chloride → HCID 86744355, compound

https://huagongshe.com/reaction/892549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 54509110HCID 54509110—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 86744355HCID 8674435592.3%

Reaction Steps

573 mg of methanesulphonyl chloride were added to a stirred solution of 1.56 g of 2-[3-(4-cyanophenoxy)-2-hydroxy-3-methylbutyl]-6-methylpyridine N-oxide in 3 ml of triethylamine and 25 ml of dichloromethane at room temperature. After 1 hour a further 573 mg of methanesulphonyl chloride were added and the mixture was stirred until thin-layer chromatography indicated that the reaction was complete. The mixture was washed with dilute hydrochloric acid and 2M sodium hydroxide solution, dried over sodium sulphate and evaporated to give 1.8 g of 2-[3-(4-cyanophenoxy)-2-methanesulphonyloxy-3-methylbutyl]-6methylpyridine N-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05118694
Source datasetuspto-grants-1992_06
ORD IDord-77e09d418cce4b92a227248688cbe3f5
Source noteuspto-grants-1992_06