HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080813Generated: October 25, 2026
Hydrazine hydrate (1:1) → 4'-Methylbiphenyl-2-carbohydrazide
https://huagongshe.com/reaction/1080813
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-(4-Methylphenyl)benzoic acid | HCID 81568 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4'-Methylbiphenyl-2-carbohydrazide | HCID 1393790 | 63% |
Reaction Steps
To a solution of 4'-methylbiphenyl-2-carboxylic acid (6.4 g) in tetrahydrofuran (50 ml) were added N,N-dimethylformamide (two drops) and oxalyl chloride (4.4 g). The mixture was stirred for 16 hours at room temperature. The solvent was evaporated to dryness under reduced pressure to give an oil, which was added dropwise to a solution of hydrazine monohydrate (7.5 g) in tetrahydrofuran (50 ml) with stirring, followed by stirring for further 6 hours. The reaction mixture was diluted with water, which was extracted with ethyl acetate. The extract was washed with water and dried. The solvent was evaporated to dryness under reduced pressure. The residue was purified by column chromatography on silica gel to give crude crystals. Recrystallization from chloroform-isopropyl ether afforded the title compound as colorless needles (4.3 g, 63%), m.p.98°-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05583141 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-5b831d7b3e6d456e83dbf3ad030a5e08 |
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| Source note | uspto-grants-1996_12 |
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