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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229757Generated: October 26, 2026

Benzyl Isothiocyanate → 4-Benzyl-1-(thiophene-2-carbonyl)thiosemicarbazide

https://huagongshe.com/reaction/229757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl IsothiocyanateHCID 2346—
ReactantThiophene-2-carbohydrazideHCID 73098—
SolventAcetonitrileHCID 6342—
Product4-Benzyl-1-(thiophene-2-carbonyl)thiosemicarbazideHCID 526068889.3%

Reaction Steps

To a hot solution of 2-thiophencarboxylic acid hydrazide (5.0 g, 35 mmol) in acetonitrile (80 mL) was added neat benzyl isothiocyanate (4.7 mL, 35 mmol) via syringe. When the solvent started to boil, the reaction vessel was removed from the heat source and allowed to cool to room temperature. The resulting crystals were collected by vacuum filtration, washed with diethyl ether and air-dried to yield N-benzyl-2-(thien-2-ylcarbonyl)hydrazinecarbothioamide (9.11 g; 89%; (M+H)+−292.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563905B2
Source datasetuspto-grants-2009_07
ORD IDord-af782016dd43493eba98f290432a7005
Source noteuspto-grants-2009_07