HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728527Generated: October 25, 2026
1,1,1-Trifluorooctan-2-YL 6-hydroxynaphthalene-2-carboxylate → Benzoic acid, 4-((1-oxodecyl)oxy)-
https://huagongshe.com/reaction/1728527
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1,1-Trifluorooctan-2-YL 6-hydroxynaphthalene-2-carboxylate | HCID 15724811 | — |
| Reactant | 1,1,1-Trifluorooctan-2-YL 2-fluoro-4-hydroxybenzoate | HCID 19920819 | — |
| Reactant | 3-Fluoro-4-(1,1,1-trifluoro-2-octyloxycarbonyl)phenyl 4-octyloxybiphenyl-4'-carboxylate | HCID 53749937 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzoic acid, 4-((1-oxodecyl)oxy)- | HCID 3608562 | — |
Reaction Steps
To a solution of the 1,1,1-trifluoro-2-octyl 6-hydroxynaphthalene-2-carboxylate (0.6 g) obtained in (1) above and the 4-n-nonylcarbonyloxybenzoic acid (0.45 g) obtained in (2) above in tetrahydrofuran (40 ml) were added dicyclohexylcarbodiimide (0.45 g) and dimethylaminopyridine (0.05 g). The solution was stirred overnight and distilled to remove the solvent. The residue was dissolved in dichloromethane (40 ml) and washed with dilute aqueous hydrochloric acid solution and water, in this order. The solution was dried over anhydrous magnesium sulfate and distilled to remove the solvent. The residue was purified by silica-gel column chromatography (developer: hexane/ethyl acetate=20/1) to obtain the titled compound (0.05 g) having specific rotation, [α]D20 =+42.86°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05328641 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-bf0e1b7dd9604ca29b4be6f68913986c |
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| Source note | uspto-grants-1994_07 |
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