HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Anisoyl chloride → N-(4-Methoxybenzoyl)benzenecarbohydrazonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Benzoic acid, 2-acetylhydrazide | HCID 256983 | — |
| Product | N-(4-Methoxybenzoyl)benzenecarbohydrazonic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06815528B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-1a042fb80e81403b884f0714e13a93e2 |
| Source note | uspto-grants-2004_11 |