HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247785Generated: October 27, 2026
Benzoic acid, 4-((1-oxodecyl)oxy)- → 4-(1,1,1-Trifluoro-2-decyloxycarbonyl)phenyl 4-n-decanoyloxybenzoate
https://huagongshe.com/reaction/247785
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoic acid, 4-((1-oxodecyl)oxy)- | HCID 3608562 | — |
| Reactant | 1,1,1-Trifluoro-2-decyl 4-hydroxybenzoate | HCID 14745754 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1,1,1-Trifluoro-2-decyloxycarbonyl)phenyl 4-n-decanoyloxybenzoate | HCID 19013920 | — |
Reaction Steps
To a solution of the 4-n-decanoyloxybenzoic acid (0.4 g) obtained in (3) and the 1,1,1-trifluoro-2-decyl 4-hydroxybenzoate (0.4 g) obtained in (2) in tetrahydrofuran (about 30 ml) were added dicyclohexylcarbodiimide (0.32 g) and dimethylaminopyridine (0.01 g). The mixture was stirred at room temperature for about 20 hours and was distilled to remove the solvent. The residue was dissolved in dichloromethane and washed with water. The organic layer was dried over anhydrous magnesium sulfate and was distilled to remove the solvent. The residue was purified by silica-gel column chromatography (a developer : hexane/ethyl acetate=20/1) to obtain the titled compound (0.15 g). Phase transition temperatures (° C.) were observed under a polarization microscope using a hot stage as follows: ##STR53## where
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05207947 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-6cfe97d6e01c4c83a1905e2fa8b45e0c |
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| Source note | uspto-grants-1993_05 |
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