HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → HCID 136360281, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | N1-bicyclo[2.2.1]hept-5-en-2-ylhydrazine-1-carbothioamide | HCID 2740681 | — |
| Product | HCID 136360281 | HCID 136360281 | — |
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-hydroxybenzaldehyde (68 mg, 0.56 mmol) similar to Example 3 and isolated as a yellow solid (47 mg, 29%). 1H NMR (CDCl3): 9.00 (s, 1H), 7.68 (s, 1H), 7.52 (d, J=8.7 Hz, 2H), 7.43 (d, J=6.9 Hz, 1H), 6.88 (d, J=8.7 Hz, 2H), 6.23-6.14 (m, 2H), 4.30-4.26 (m, 1H), 3.05 (s, 1H), 2.96 (s, 1H), 1.94-1.86 (m, 1H), 1.66 (d, J=9.0 Hz, 1H), 1.51 (d, J=9.0 Hz, 1H), 1.45-1.38 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794400B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-3d04c94189524482884a8e0e9d198455 |
| Source note | uspto-grants-2004_09 |