HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Chlorophenyl)hydrazine → HCID 72557542, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Chlorophenyl)hydrazine | HCID 70624 | — |
| Reactant | 1-Indanone, 6-bromo- | HCID 139778 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 72557542 | HCID 72557542 | 101.5% |
Reaction Steps
To a mixture of 6-Bromo-indan-1-one (0.58 g, 2.7 mmole) in ethyl alcohol (5 mL) was added (4-Chloro-phenyl)-hydrazine (0.492 g, 2.7 mmole) and 5 drops of acetic acid. The reaction mixture was refluxed for 30 minutes then cooled to room temperature. The resulting solid precipitate was filtered and washed with ice cold methanol to give N-(6-Bromo-indan-1-ylidene)-N′-(4-chloro-phenyl)-hydrazine (0.92 gm, 100%). HPLC Rt=4.69 min. m/z=335 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07417040B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-90df0b48e84f452188df3d3c7c3e5547 |
| Source note | uspto-grants-2008_08 |