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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721549Generated: October 30, 2026

Benzaldehyde → HCID 2851580, compound

https://huagongshe.com/reaction/1721549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantWaterHCID 962—
ReactantHydrazine, 1,1-diphenyl-, hydrochloride (1:1)HCID 10738—
SolventTetrahydrofuranHCID 8028—
ProductHCID 2851580HCID 2851580—

Reaction Steps

In 500 parts of tetrahydrofuran were dissolved 23.8 parts of 4- 5-(5H-dibenzo b,f!azepinyl)!benzaldehyde and 26.5 parts of N,N-diphenylhydrazine hydrochloride. This solution was stirred at room temperature for 3 hours. After completion of the reaction, the reaction mixture was poured into 2,000 parts of water, and the crystals precipitated were taken out by filtration. The crystals obtained were washed with ethyl alcohol and then dried at reduced pressure. The crystals dried were dissolved in 100 parts of ethyl acetate, and this solution was poured into 1,000 parts of methyl alcohol to recrystallize the reaction product. Thus, 28.9 parts (yield, 77.9%) of 4- 5-(5H-dibenzo b,f!azepinyl)!benzaldehyde N,N-diphenylhydrazone was obtained. This compound had a melting point of 178.0° to 179.0° C. The results of elemental analysis are shown in Table 4 below, together with calculated values for C33H25N3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512400
Source datasetuspto-grants-1996_04
ORD IDord-cfab5c85a06d47b5bcc35dda12acf548
Source noteuspto-grants-1996_04