Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylimidazole | HCID 12749 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86618677 | HCID 86618677 | — |
| Solvent | Diethylene Glycol | HCID 8117 | — |
| Product | HCID 68454783 | HCID 68454783 | 89% |
Reaction Steps
A mixture of α-(4′-chlorophenyl)-4-acetyloxy-3-methoxy cinnamic acid (0.0083 mol), NaHCO3 (10%, 5 mL) and methylimidazole (2 mL) and diethylene glycol (8 mL) were taken in a 100 ml round bottom flask fitted with a condenser. The flask was shaken well and placed inside the microwave oven and irradiated (200 W, 180° C.) for 9 minutes in parts. After completion of reaction, the reaction mixture was worked (yield 89%) as in example I; solid, (m.p. 121-124° C.); 1H NMR (CDCl3) δ 7.35 (2H, d, J=8.48 Hz), 7.25 (2H, d, J=8.07 Hz), 6.96 (3H, m), 6.87 (2H, d, J=8.07 Hz), 5.72 (1H, s), 3.87 (3H, s); 13C NMR (CDCl3) δ 146.8, 145.8, 136.1, 132.7, 129.6, 129.2, 128.8, 127.4, 125.1, 120.6, 114.6, 108.3 and 55.9. HREIMS data: m/z [M+H]+ for C15H14O2Cl, calculated=261.7229; observed=261.7228.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759527B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-0fc1fb90029c462eb035f00fbdb35ff4 |
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| Source note | uspto-grants-2010_07 |
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