HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromophenylhydrazine hydrochloride → HCID 46098126, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromophenylhydrazine hydrochloride | HCID 12157 | — |
| Reactant | 2-Methyl-N-(4-oxocyclohexyl)propanamide | HCID 21533994 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 46098126 | HCID 46098126 | 77% |
Reaction Steps
Combine p-bromophenylhydrazine hydrochloride (10.0 g, 44.7 mmol) and N-(4-oxo-cyclohexyl)isobutyramide (8.20g, 44.7 mmol) in saturated ethanolic HCl (180 mL) and heat at reflux under nitrogen for 18 h. Concentrate in vacuo to remove about ½ of the EtOH, then dilute with water (300 mL). Collect the resulting solid, slurry in EtOAc and recollect to give 11.5 g (77%) of a beige solid. MS (ES): 335 (M+1), 337 (M+H+2). 1H NMR(DMSO-d6): δ 10.93 (s, 1H, NH), 7.80 (d, 1H, J=7.9 Hz), 7.48 (s, 1H), 7.19 (d, 1H, J=8.8 Hz), 7.07 (d, 1H, J=8.4 Hz), 4.00 (m, 1H), 2.86 (dd, 1H, J=15.2, 5.1 Hz), 2.77 (m, 2H), 2.46-2.32 (m, 2H), 1.93 (m, 1H), 1.75 (m, 1H), 0.99 (d, 6H, J=6.6 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935722B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-ccc98e5f1e3542a0957e368c9b048259 |
| Source note | uspto-grants-2011_05 |