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 (3×) 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): δ1.23(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 | US05030736 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-b8ecc40979eb4114b8b578d79eaf3a92 |
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| Source note | uspto-grants-1991_07 |
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