HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 14986508, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-(Trifluoromethyl)benzamide | HCID 74684 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 6-bromo-5,6-dihydro-7-hydroxy-5,5-dimethyl-7H-thieno[3,2-b]pyran | HCID 14986486 | — |
| Product | HCID 14986508 | HCID 14986508 | — |
Reaction Steps
The title compound was prepared as described in Example 3 starting with 6-bromo-7-hydroxy-5,6-dihydro-5,5-dimethyl-7H-thieno[3,2-b]pyran (4.5 g, 17.1 mmol) and 4-trifluoromethylbenzamide (7.43 g, 39.3 mmol) in N,N-dimethylformamide (75 mL) to give the product, 1.96 g (31%), as a colorless solid: mp 162°-163° C.; IR (KBr): 3396, 1664, 1534 and 1507 cm-1 ; MS: m/z 372 (MH+); 1H NMR (DMSO-d6): δ 1.21 (s, 3H), 1.40 {s, 3H), 3.80 (m, 1H, simplifies to d, J=8.7 Hz, with D2O), 5.01 (m, 1H, simplifies to d, J=8.7 Hz, with D2O), 5.68 (d, J=6.0 Hz, 1H, exchanges with D2O), 6.59 (d, J=5.7 Hz, 1H), 7.31 (d, J= 5.7 Hz, 1H), 7.88 (d, J=8.3 Hz, 2H), 8.11 (d, J=8.3 Hz, 2H) and 9.05 (d, J=8.4 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-660b96a3204a42aba86d70984ecb263e |
| Source note | uspto-grants-1993_11 |