HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → [1-(4-Trifluoromethoxyphenyl)-methylidene]-hydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | p-(Trifluoromethoxy)benzaldehyde | HCID 69573 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | [1-(4-Trifluoromethoxyphenyl)-methylidene]-hydrazine | HCID 66679788 | 91% |
Reaction Steps
Hydrazine (3.3 mL, 105 mmol) was dissolved in ethanol (10 mL) at room temperature. To this solution was added 4-trifluoromethoxybenzaldehyde (5.0 mL, 35 mmol) dropwise over 25 min. The reaction mixture was stirred an additional 45 min and concentrated under vacuum. The residue was dissolved in ethyl ether (20 mL) and washed with water (10 mL). The water layers were extracted with ethyl ether (3×15 mL), and the combined organic layer was dried over magnesium sulfate, filtered and concentrated to give [4-(trifluoromethoxy)benzylidene]hydrazine (XX) as a yellow oil (6.5 g, 91% yield). 1H NMR (DMSO-d6): δ 7.69 (s, 1H); δ 7.56 (d, J=8.7 Hz, 2H) δ 7.30 (d, J=7.8 Hz, 2H); δ 6.94 (bs, 2H); GC-MS m/z 204 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08067588B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-c02e39242dcd45e7a2a591a0202b05ee |
| Source note | uspto-grants-2011_11 |