HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzaldehyde → 4-(Bicyclo[2.2.1]hept-5-en-2-yl)-1-(4-chlorobenzylidene)thiosemicarbazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | N1-bicyclo[2.2.1]hept-5-en-2-ylhydrazine-1-carbothioamide | HCID 2740681 | — |
| Product | 4-(Bicyclo[2.2.1]hept-5-en-2-yl)-1-(4-chlorobenzylidene)thiosemicarbazide | HCID 73996746 | — |
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 4-chlorobenzaldehyde (79 mg, 0.56 mmol) similar to Example 3 and isolated as a white solid (68 mg, 40%). 1H NMR (CDCl3): 9.15 (s, 1H), 7.73 (s, 1H), 7.56 (d, J=8.4 Hz, 2H), 7.44 (s, 1H), 7.39 (d, J=8.7 Hz, 2H), 6.24-6.14 (m, 2H), 4.30-4.25 (m, 1H), 3.06 (s, 1H), 2.97 (s, 1H), 1.95-1.87 (m, 1H), 1.68 (d, J=9.0 Hz, 1H), 1.51 (d, J=9.0 Hz, 1H), 1.45-1.39(m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794400B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-504aff9a9b54405e8bedcf5923eb3409 |
| Source note | uspto-grants-2004_09 |