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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612843Generated: October 31, 2026

Water → 5-(4-Methoxyphenyl)thiophene-2-carbohydrazide

https://huagongshe.com/reaction/612843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHydrazineHCID 9321—
ReactantThionyl ChlorideHCID 24386—
Reactant5-(4-methoxyphenyl)thiophene-2-carboxylic AcidHCID 2764130—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product5-(4-Methoxyphenyl)thiophene-2-carbohydrazideHCID 276358478.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1.8 g (7.7 mmol) of the thienoic acid in 1 mL of dry DMF and 30 mL of toluene is added 1.1 mL (15.4 mmol) of thionyl chloride and the mixture is heated at 80° C. for 3 hours. After cooling to room temperature, the solvent and excess thionyl chloride are removed under reduced pressure. The resulting residue is dissolved in 50 mL of dry THF and is added dropwise over a period of 30 minutes into a solution of 4.8 mL (154 mmol) of anhydrous hydrazine in 100 mL of dry THF while stirring at -30° C. After stirring at room temperature for 2 hours, 100 mL of water is added to the reaction mixture. The desired product is extracted with chloroform (4×100 mL), dried over anhydrous Na2SO4 and concentrated to give 1.5 g (75%) of 5-(4-methoxyphenyl)-2-thienoylhydrazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06005113
Source datasetuspto-grants-1999_12
ORD IDord-f4ce38766c9744fc822c8a421c4b26f8
Source noteuspto-grants-1999_12