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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627826Generated: November 3, 2026

Benzoylhydrazine → HCID 86693873, compound

https://huagongshe.com/reaction/627826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoylhydrazineHCID 11955—
ReactantHCID 86693874HCID 86693874—
Solvent1-ButanolHCID 263—
ProductHCID 86693873HCID 8669387358%

Reaction Conditions

Temperature120 °C

Reaction Steps

Into a 100-mL three-neck flask were put the total amount of N-[(ethylsulfanyl)(2-methylphenyl)methylidene]methylamine obtained in Step 3, 7.0 g (51.4 mmol) of benzoylhydrazine, and 30 mL of 1-butanol (1-BuOH), and the mixture was heated and stirred at 120° C. for 15 hours. After reaction for the predetermined time, the solvent was distilled off to give a yellow liquid. This liquid was purified by silica gel chromatography. Ethyl acetate was used as a developing solvent. The obtained fraction was concentrated to give a white solid. This solid was recrystallized with ethyl acetate, so that 7.0 g of a white solid of Hmpptz-Me (abbreviation), an objective 4H-triazole derivative, was obtained in a yield of 58%. A synthesis scheme of Step 4 is shown in (f-4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309458B2
Source datasetuspto-grants-2016_04
ORD IDord-f0446b841509480cbc01dfd976f41641
Source noteuspto-grants-2016_04