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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443449Generated: October 25, 2026

Hexane → 3-(m-Trifluoromethylbenzylmercapto)-2,5-pyridine-dicarboxylic acid dimethyl ester

https://huagongshe.com/reaction/443449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantSodium hydrideHCID 24758—
Reactant3-(Trifluoromethyl)benzyl mercaptanHCID 141236—
Reactant3-Nitro-2,5-pyridinedicarboxylic acid dimethyl esterHCID 53975227—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-(m-Trifluoromethylbenzylmercapto)-2,5-pyridine-dicarboxylic acid dimethyl esterHCID 54024789—

Reaction Steps

The solution of 4.6 g of m-trifluoromethylbenzylmercaptan in 30 ml of dimethylformamide is added to the slurry of 1.08 g of 50% sodium hydride in mineral oil (washed 2 times with hexane), under nitrogen while stirring at room temperature. After several minutes, a clear yellow solution is obtained, which is combined with that of 5.0 g of 3-nitro-2,5-pyridinedicarboxylic acid dimethyl ester in 50 ml of dimethylformamide. The mixture is warmed on the steam bath for 30 minutes at 90° and stirred at room temperature overnight. It is acidified with 2 ml of acetic acid and diluted to 400 ml with a mixture of ice and water. The precipitate formed is collected and recrystallized from methanol-diethyl ether (1:1), to yield the 3-(m-trifluoromethylbenzylmercapto)-2,5-pyridine-dicarboxylic acid dimethyl ester melting at 102°-106°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04260620
Source datasetuspto-grants-1981_04
ORD IDord-efd756ed420344f197f24e94481a5b3d
Source noteuspto-grants-1981_04