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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269468Generated: October 26, 2026

Pyridine → N-[4-cyano-3-trifluoromethyl-phenyl]-2-hydroxy-3-methanesulfonyloxy-2-methyl-propionamide

https://huagongshe.com/reaction/1269468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN-[4-cyano-3-(trifluoromethyl)phenyl]-2,3-dihydroxy-2-methylpropanamideHCID 9882395—
SolventDichloromethaneHCID 6344—
ProductN-[4-cyano-3-trifluoromethyl-phenyl]-2-hydroxy-3-methanesulfonyloxy-2-methyl-propionamideHCID 12148451—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 46 g (0.16 mol) of N-[4-cyano-3-trifluoromethyl-phenyl]-2,3-dihydroxy-2-methyl-propionamide in 1 1 of dichloromethane and 46 ml (0.57 mol) of dry pyridine was cooled to 0° C. and 46 ml (0.59 mol) of methanesulfonyl chloride was added dropwise. The mixture was stirred at 0° C. for 5 h, then washed three times with 500 ml of saturated aqueous sodium hydrogen carbonate, 500 ml of 10% aqueous hydrochloric acid and 500 ml of brine. The organic layer was dried over sodium sulfate and concentrated in vacuum. The residue was crystallized with 200 ml of petroleum ether, which has a boiling range of 40–70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199257B1
Source datasetuspto-grants-2007_04
ORD IDord-b35866d175fd4d758effefbba81c681b
Source noteuspto-grants-2007_04