Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 14986504 | HCID 14986504 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14986505 | HCID 14986505 | — |
Reaction Steps
6-Acetoxy-2-acetyl-5,6-dihydro-5,5-dimethyl-7-(4-nitrobenzamido)-7H-thienopyran (0.60 g, 1.39 mmol) was treated with aqueous sodium hydroxide (1N, 1.5 mL, 1.5 mmol) in methanol (10 mL) at rt and stirred for 2 h. The resultant solution was poured into water and extracted with 5% isopropanol in dichloromethane. The organic phase was washed with water (3x) and dried over magnesium sulfate. The solvent was evaporated in vacuo and the resultant solid triturated in diethyl ether to give the product, 0.36 g (66%), as a pale yellow solid: mp 223°-225° C.; IR (KBr): 1647, 1601, 1530 and 1458 cm-1 ; MS: m/z 391 (MH+); 1H NMR (DMSO-d6): δ 1.23 (s, 3H), 1.42 (s, 3H), 2.45 (s, 3H), 3.84 (m, 1H, simplifies to d, J=8.9 Hz with D2O), 5.01 (m, 1H, simplifies to d, J=8.9 Hz, with D2O), 5.86 (d, J=5.9 Hz, 1H, exchanges with D2O), 7.47 (s, 1H), 8.14 (d, J=8.8 Hz, 2H), 8.36 (d, J=8.8 Hz, 2H) and 9.27 (d, 1H, exchanges with D2O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04992435 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-b12d0e13c8fa4f7ca585d0ce7cb26038 |
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| Source note | uspto-grants-1991_02 |
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