HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Trifluoromethyl)benzaldehyde → HCID 73996747, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Trifluoromethyl)benzaldehyde | HCID 67996 | — |
| Reactant | N1-bicyclo[2.2.1]hept-5-en-2-ylhydrazine-1-carbothioamide | HCID 2740681 | — |
| Product | HCID 73996747 | HCID 73996747 | — |
Reaction Steps
The title compound was prepared from a mixture of N1-bicyclo[2.2.1]hept-5-en-2-ylhydrazine-1-carbothioamide (100 mg, 0.56 mmol) and α,α,α-trifluoro-p-tolualdehyde (76 μL, 0.56 mmol) similar to Example 3 and isolated as a white solid (60 mg, 32%). 1H NMR (CDCl3): 9.14 (s, 1H), 7.78 (s, 1H), 7.73 (d, J=8.7 Hz, 2H), 7.67 (d, J=8.7 Hz, 2H), 7.46 (d, J=7.2 Hz, 1H), 6.25-6.14 (m, 2H), 4.30-4.26 (m, 1H), 3.07 (s, 1H), 2.98 (s, 1H), 1.96-1.88 (m, 1H), 1.69 (d, J=9.0 Hz, 1H), 1.51 (d, J=8.7 Hz, 1H), 1.46-1.40(m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794400B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-ae97324cfaf54aac97c4dcb0ae80abb5 |
| Source note | uspto-grants-2004_09 |