Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 3-(3,4-Dihydroxybenzoyl)-benzoic acid | HCID 18963081 | — |
| Product | HCID 53980466 | HCID 53980466 | — |
Reaction Steps
A solution of 2.9g of 3-(3,4-dihydroxybenzoyl)-benzoic acid in 100 ml of methanol is mixed with 7g of Amberlyst 15® and refluxed with stirring for 8 hours. The reaction mixture is filtered on diatomaceous earth, the filtrate concentrated by evaporation, taken up in ethyl acetate and shaken out with 10% sodium bicarbonate solution. The organic phase is dried on sodium sulfate and concentrated by evaporation. 1.4g of 3-(3,4-dihydroxybenzoyl)-benzoic acid methyl ester is obtained as oily crude product. 272 mg of this crude product is dissolved in 2.5 ml of dimethylformamide, mixed with 269 mg of (1E)-6-bromo-l-(4-methoxyphenyl)-1-hexene and 185 mg of lithium carbonate and the mixture is heated for 18 hours to 50°-60° C. with stirring. The reaction mixture is filtered, washed with dichloromethane, the filtrate is concentrated by evaporation and the residue is chromatographed on silica gel with hexane/ethyl acetate=98/2. 230 mg of 3-[3-hydroxy- 4-[6-(4-methoxyphenyl)-(5E)-5-hexenyloxy]benzoyl]-benzoic acid methyl ester is obtained as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05352701 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-e51571d0e34044a291687ca19ea27160 |
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| Source note | uspto-grants-1994_10 |
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