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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333201Generated: October 29, 2026

p-Toluenesulfonic acid → 1-(3-Methylbenzoyl),3-(3-methylbenzoyl)benzene thiosemicarbazone

https://huagongshe.com/reaction/333201

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantThiosemicarbazideHCID 2723789—
Reactant1-(3-Methylbenzoyl),3-(3-methylbenzoyl)benzeneHCID 54177246—
SolventMethanolHCID 887—
Product1-(3-Methylbenzoyl),3-(3-methylbenzoyl)benzene thiosemicarbazoneHCID 7816524917%

Reaction Steps

p-toluenesulfonic acid (0.018 g, 0.09 mmol) was added to a solution of 1-(3-methylbenzoyl),3-(3-methylbenzoyl)benzene 8 (0.300 g, 0.95 mmol) in anhydrous methanol (10 mL). After stirring at reflux for 10 min, thiosemicarbazide (0.086 g, 0.954 mmol) was added to the reaction mixture and stirred for 12 h under an inert atmosphere of nitrogen gas. After 12 h, methanol was removed under reduced pressure and 10 mL of water was then added. The products were extracted with dichloromethane (2×30 mL) and the combined organic phases were washed with brine, dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. Purification using flash chromatography (silica gel, hexanes:ethyl acetate, gradient 90:10 to 80:20) afforded 1-(3-methylbenzoyl),3-(3-methylbenzoyl)benzene thiosemicarbazone 9 (0.063 g, 0.016 mmol) as a white solid in a 17% yield. HRMS (ESI) calculated for C23H21N3OSH+ (M+H)+ 388.14781, found 388.14793. The product was determined to be approximately 80% pure and was submitted for biological testing without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877967B2
Source datasetuspto-grants-2014_11
ORD IDord-3ad2deb1d07d4cb89faca29f27fbf6b4
Source noteuspto-grants-2014_11