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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266301Generated: November 1, 2026

Benzylhydrazine dihydrochloride → HCID 178515600, compound

https://huagongshe.com/reaction/2266301

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). HPLC/MS (method A): retention time=3.29 min, (M+H)+=313.1. 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 numberUS07858639B2
Source datasetuspto-grants-2010_12
ORD IDord-9c864979b3224d53a3c3f3886cd0b8a4
Source noteuspto-grants-2010_12