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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700555Generated: November 2, 2026

Hydrochloric Acid → 2-[(E)-[6-(4-fluorophenyl)-3-methyl-6,7-dihydro-5H-1-benzofuran-4-ylidene]amino]guanidine;hydrochloride

https://huagongshe.com/reaction/1700555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant6-(4-Fluorophenyl)-3-methyl-4,5,6,7-tetrahydrobenzofuran-4-oneHCID 18317673—
ReactantHCID 178418668HCID 178418668—
SolventEthanolHCID 702—
Product2-[(E)-[6-(4-fluorophenyl)-3-methyl-6,7-dihydro-5H-1-benzofuran-4-ylidene]amino]guanidine;hydrochlorideHCID 17843114072.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of 6-(4-fluorophenyl)-3-methyl-4,5,6,7-tetrahydrobenzofuran-4-one (0.12 g) and aminoguanidine hydrochloride (59 mg) were added ethanol (10 ml) and 6N hydrochloric acid (0.046 ml), and the mixture was stirred at 90° C. for 1 hour and cooled. The reaction solution was concentrated under reduced pressure, and the residue was washed with ethanol and isopropylether, and dried to give (E)-6-(4-fluorophenyl)-4-guanidinoimino-3-methyl-4,5,6,7-tetrahydrobenzofuran hydrochloride (Compound 34) (0.12 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350749B1
Source datasetuspto-grants-2002_02
ORD IDord-715099253734475c81e6521d85f9d913
Source noteuspto-grants-2002_02