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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613685Generated: October 25, 2026

4-Chloro-1-(2-thienyl)butan-1-one → 2-[4-Chloro-1-(thiophen-2-yl)-butylidene]-hydrazinecarbothioamide

https://huagongshe.com/reaction/613685

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-1-(2-thienyl)butan-1-oneHCID 123511—
ReactantThiosemicarbazideHCID 2723789—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-[4-Chloro-1-(thiophen-2-yl)-butylidene]-hydrazinecarbothioamideHCID 5456960957%

Reaction Steps

Thiosemicarbazide (9.11 g, 0.1 mol) was added under nitrogen to a solution 4-chloro-2'-butyrothienone (16.2 mL, 0.1 mol) in 350 mL of methanol plus 27 mL 1N HCl plus 25 mL of water. After stirring at room temperature for approximately 2 hours, all of the solid had dissolved. The reaction was then stirred at room temperature for 24 hours (overnight). By TLC starting material remained. An additional 27 mL of 1N HCl was added and the reaction stirred at room temperature for 6 hours. The solid formed was removed by filtration and dried under high vacuum to give 14.87 g (57%) of the title compound as a brown solid, mp 120-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008362
Source datasetuspto-grants-1999_12
ORD IDord-08f667f3cc214dae90b9d0e45627e7c1
Source noteuspto-grants-1999_12