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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250341Generated: October 30, 2026

Benzylhydrazine dihydrochloride → HCID 178515600, compound

https://huagongshe.com/reaction/2250341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylhydrazine dihydrochlorideHCID 146540—
Reactant3-(4-Chlorophenyl)-2,5-furandioneHCID 585997—
SolventAcetic AcidHCID 176—
ProductHCID 178515600HCID 178515600—

Reaction Steps

To a suspension of 3-(4-chlorophenyl)-2,5-furandione (10.24 g, 66.9 mmol) in acetic acid (300 mL) was added benzylhydrazine dihydrochloride in one portion (19.6 g, 100 mmol). The reaction mixture was stirred at reflux for 14 h. Analysis by HPLC/MS indicated the reaction was complete. After cooling to room temperature, the resulting white suspension was filtered. The collected solid was washed with EtOAc (20 mL×2), and dried in a 50° C. vacuum oven for 16 h to yield 6.5 g of the desired product as a white solid. The filtrate was concentrated under reduced pressure, and the obtained residue was crystallized in EtOAc to afford additional 1.6 g of the title compound (8.1 g in total, 39% yield). LC/MS (method A): retention time=3.30 min, (M+H)+=313. 1H NMR (DMSO-d6, 500 MHz): δ 11.62 (s, 1H), 7.65 (d,J=10 Hz, , 2H), 7.51 (d,J=10 Hz, 2H), 7.23-7.38 (m, 5H), 7.04 (s, 1H), 5.11 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317012B2
Source datasetuspto-grants-2008_01
ORD IDord-25d6d7d5ed26419c9d3e577a49c12586
Source noteuspto-grants-2008_01