Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | HCID 23296053 | HCID 23296053 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70021349 | HCID 70021349 | — |
Reaction Steps
12.7 g of methyl 3-(2-methylenecyclopentyloxy)-4-methoxybenzoate are treated with 50 ml of quinoline and the mixture is stirred at 190° C. for 1 h. After cooling, it is treated with water, adjusted to pH 3 using 2N HCl and extracted with ethyl acetate. The residue which remains after concentrating the solvent is chromatographed on a silica gel column using ethyl acetate/petroleum ether (4:6). The chromatographically pure fractions are concentrated and dried in a high vacuum. 10.2 g of the title compound are obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06121274 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-6448ff006e5b4b529607312efb8b4c9c |
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| Source note | uspto-grants-2000_09 |
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