Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cornforth reagent | HCID 2724130 | — |
| Reactant | HCID 69492813 | HCID 69492813 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10287620 | HCID 10287620 | 75.3% |
Reaction Steps
4-[3-(2,4-Dimethoxy-5-thiophen-2-yl-phenyl)-1-hydroxy-prop-2-ynyl]-benzoic acid methyl ester (2.0 g, 4.90 mmol) from Ex-1C was dissolved in dichloromethane (60 mL). Pyridinium dichromate (3.70 g, 9.8 mmol) was added and the resulting mixture was stirred at room temperature under nitrogen for 5 h. The reaction was then filtered through a pad of celite and concentrated under reduced pressure. Silica gel chromatography (dichloromethane/methanol, 30:1) gave 1.5 g (75%) of the desired 4-[3-(2,4-dimethoxy-5-thiophen-2-yl-phenyl)-propynoyl]-benzoic acid methyl ester as a yellow solid, m.p. 198–200° C. 1H-NMR (300 MHz, CDCl3) δ 8.38 (d, 2H, J=8.0 Hz), 8.17 (d, 2H, J=8.0 Hz), 0.88 (s, 1H), 7.41 (dd, 1H, J=3.7 and 1.6 Hz), 7.33 (dd, 1H, J=5.2 and 1.6 Hz), 7.09 (dd, 1H, J=5.2 and 3.7 Hz), 6.55 (s, 1H), 4.05 (s, 3H), 4.01 (s, 3H), 4.00 (s, 31H); EIMS m/z 406 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202247B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-dee0159f7cb143f1ace42486d32c270a |
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| Source note | uspto-grants-2007_04 |
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