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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623823Generated: November 3, 2026

3-Fluoro-5-(trifluoromethyl)benzonitrile → 3-(Methylthio)-5-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/623823

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-5-(trifluoromethyl)benzonitrileHCID 519037—
ReactantSodium methanethiolateHCID 4378561—
ReactantDichloromethane methanolHCID 21226129—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product3-(Methylthio)-5-(trifluoromethyl)benzamideHCID 70557756—

Reaction Steps

In a 500-mL, 3-neck round-bottomed flask equipped with an 100-mL pressure-equalizing addition funnel fitted with an nitrogen inlet, and a rubber septum, 3-fluoro-5-(trifluoromethyl)benzonitrile (8.0 g, 1.0 eq.), in acetone (40 mL). Sodiumthiomethoxide (3.42 g, 1.15 eq) was dissolved in water to make 21% aqueous solution and was added dropwise in 30 min at 5° C. temperature. The temperature of the reaction was slowly raised to RT and stirred for 3 h. Then temperature was raised to 50-60° C. and maintained for further 4-6 h. The progress of the reaction was followed by TLC analysis on silica gel with 10% MeOH-dichloromethane as mobile phase and visualization with UV, SM Rf=0.40 and Product Rf=0.25. Reaction was stirred for 3 hr at 25° C. and 4-6 hrs at 50-60° C. and reaction mixture was transparent. The reaction mass was quench by water and extracted by ethyl acetate (3×100 mL). The combined organic layer was washed with brine 50 mL and dried over sodium sulphate and evaporated on buchi rotaevaporator. The resulting crude compound (8 g) was subjected to further stage Yield (80.9%); Mass: (ES+) 235.94 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303000B2
Source datasetuspto-grants-2016_04
ORD IDord-55b7f741b3ed4f92bd9a83d8c73f4045
Source noteuspto-grants-2016_04