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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414854Generated: November 3, 2026

p-Anisoyl chloride → N-(4-Methoxybenzoyl)benzenecarbohydrazonic acid

https://huagongshe.com/reaction/2414854

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantBenzoic acid, 2-acetylhydrazideHCID 256983—
ProductN-(4-Methoxybenzoyl)benzenecarbohydrazonic acidHCID 258695—

Reaction Steps

Synthesis and isolation were same as 1-acetyl-2-benzoylhydrazine, using 1.5 g (11.2 mmol) of benzoylhydrazide, 1.9 g (11.1 mmol) of 4-methoxybenzoylchloride and 1.1 g of TEA. Yield was 2.9 g (97%). 1H NMR (200 MHz, d6-DMSO) δ 5.13 (s, 3H), 8.36 (d, 2H), 8.86 (m, 3H), 9.23 (d, 4H) 11.72 (d, 2H); MS (EI, m/e, relative intensity %) calcd for C15H14N2O3 270, found 270 (M+, 5.1); mp 201-202° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06815528B2
Source datasetuspto-grants-2004_11
ORD IDord-1a042fb80e81403b884f0714e13a93e2
Source noteuspto-grants-2004_11