Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 6-Hydroxy-2-naphthoic acid | HCID 85557 | — |
| Reactant | 4-Octyloxybenzoyl chloride | HCID 2760250 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19013137 | HCID 19013137 | 88% |
Reaction Steps
In 30 ml of dichloromethane, 3 g of 6-hydroxy-2-naphthoic acid and 2.4 g oftriethylamine were dissolved. To this solution were added 4.4 g of 4-octyloxybenzoic acid chloride and 0.2 g of dimethylaminopyridine, and the solution was stirred for about 20 hours at an ambient temperature. A diluted hydrochloric acid solution was added to the solution and the organic layer in the mixed solution was separated by means of a separatingfunnel. After the solvent was distilled off, the residue was washed with n-hexane and dried to obtain 5.9 g of 6-(4-octyloxyphenylcarbonyloxy)-2-naphthoic acid. The compound was added in 10 g of thionyl chloride to dissolve, and a very small amount of N,N-dimethyl formamide was added to the solution and the solution was refluxed for 4 hours. An excess amount of thionyl chloride was distilled off to obtain 5.7 g of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05330678 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-8b5218cd00834320b287ebf85a6d801e |
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| Source note | uspto-grants-1994_07 |
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