Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Veratrole | HCID 7043 | — |
| Reactant | 2,6-Dimethoxybenzoyl chloride | HCID 74810 | — |
| Reactant | Bis(3,4-dimethoxyphenyl)methanone | HCID 223042 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | HCID 21584605 | HCID 21584605 | — |
Reaction Steps
2′,6′,3,4-Tetramethoxybenzophenone was prepared analogously to 3,4,3′,4′-tetramethoxybenzophenone except using veratrole (1.3 mL, 10 mmol), aluminum chloride (1.47 g, 11 mmol) and 2,6-dimethoxybenzoyl chloride (2.0 mL, 10 mmol) with a reaction time of 24 hours at room temperature. The crude mixture was purified by flash column chromatography (silica gel, 4% ethyl acetate/methylene chloride) to afford 2.11 g (70%) of the product as a white solid: mp 128–129° C.; 1H NMR (CDCl3) δ 7.66–7.60 (m, 1H), 7.40–7.20 (m, 2H), 6.88–6.79 (m, 1H), 6.67–6.65 (m, 2H), 3.93 (s, 3H), 3.91 (s, 3H), 3.71 (s, 6H); 13C NMR (CDCl3) δ 193.8, 157.4, 153.4, 148.9, 130.9, 130.5, 125.3, 118.0, 110.2, 109.9, 104.0, 55.9, 55.8; Anal. Calcd for C17H18O5. Theoretical: C, 67.54; H, 6.00. Found: C, 66.51; H, 5.91.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07019030B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-abd1c35454af412aa0b6ebd2e548fa8c |
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| Source note | uspto-grants-2006_03 |
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