HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → HCID 14986507, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 7-(4-Chlorobenzamido)-5,6-dihydro-6-hydroxy-5,5-dimethyl-7H-thieno[3,2-b]pyran | HCID 14986506 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 14986507 | HCID 14986507 | — |
Reaction Steps
The title compound was prepared as described in Example 9 starting with 7-(4-chlorobenzamido)-5,6-dihydro-6-hydroxy-5,5-dimethyl-7H-thieno[3,2-b]pyran (1.23 g, 3.64 mmol) and 90% nitric acid (1.5 mL) in acetic acid (20 mL) to give the product, 0.384 g (28%), as a yellow solid: mp 226°-229° C. dec; IR (KBr): 3315, 1655, 1535 and 1503 cm-1;MS: m/z 383 (MH+); 1H NMR (DMSO-d6): δ 1.25 (s, 3H), 1.44 (s, 3H), 3.90 (m, 1H, simplifies to d, J=8.9 Hz with D2O), 4.95 (m, 1H, simplifies to d, J=8.9 Hz, with D2O), 5.94 (d, J=6.0 Hz, 1H exchanges with D2O), 7.60 (d, J=8.6 Hz, 2H), 7.72 (s, 1H), 7.94 (d, J=8.6 Hz, 2H) and 9.11 (d, J=7.6 Hz, 1H, exchanges with D2O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05260453 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-56a7be2c24d2450aa4ce43d4cb18f942 |
| Source note | uspto-grants-1993_11 |