Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 23296057 | HCID 23296057 | — |
| Product | HCID 23296051 | HCID 23296051 | — |
Reaction Steps
20 g of methyl 4-methoxy-3-(2-methyl-2-propenyloxy)benzoate are dissolved in 60 ml of quinoline and the mixture is heated at 180-190° C. for 2 h. After cooling, it is treated with ethyl acetate and the quinoline is extracted using 2N HCl. The organic phase is washed a further 2 times with water and concentrated. The oily residue is chromatographed on a silica gel column using ethyl acetate/petroleum ether (4:6). The chromatographically pure fractions are combined, concentrated and dried in a high vacuum. 15.6 g of the title compound are obtained as a pale 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-e9f9b6f73970403db1776cf9970662d2 |
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| Source note | uspto-grants-2000_09 |
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