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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703345Generated: October 29, 2026

Benzaldehyde → HCID 178513837, compound

https://huagongshe.com/reaction/703345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantWaterHCID 962—
ReactantHCID 54137908HCID 54137908—
SolventAcetic AcidHCID 176—
ProductHCID 178513837HCID 178513837—

Reaction Steps

In 0.7 ml of acetic acid, 245 mg (0.6 mmol) of oxamide 4-chloro-3-[(2,2,-3,3,4,4,4-heptafluorobutoxy)methyl]phenylhydrazone was dissolved and nitrogen was saturated. The solution was added with 76 mg (0.72 mmol) of benzaldehyde under a nitrogen atmosphere and stirred at room temperature for 16 hours. Then water was added to the solution and the formed crystals were filtered out, washed with water and dried in vacuo. The resulting product was recrystallized from ethyl acetate/n-hexane with nitrogen saturated to obtain 257 mg (86.5% yield) of 1-[4-chloro-3-](2,2,3,3,4,4,4-heptafluorobutoxy)methyl]phenyl]-4,5-dihydro-5-phenyl-1H-1,2,4-triazole-3-carboxamide (m.p. 157°-159° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983209
Source datasetuspto-grants-1991_01
ORD IDord-91e2d9cc89ce43f986e519e3139e8118
Source noteuspto-grants-1991_01