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HRID 247785作成日:2026年10月26日
Benzoic acid, 4-((1-oxodecyl)oxy)- → 4-(1,1,1-Trifluoro-2-decyloxycarbonyl)phenyl 4-n-decanoyloxybenzoate
https://huagongshe.com/reaction/247785
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzoic acid, 4-((1-oxodecyl)oxy)- | HCID 3608562 | — |
| 反応物 | 1,1,1-Trifluoro-2-decyl 4-hydroxybenzoate | HCID 14745754 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-(1,1,1-Trifluoro-2-decyloxycarbonyl)phenyl 4-n-decanoyloxybenzoate | HCID 19013920 | — |
反応手順
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
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05207947 |
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| 出典データセット | uspto-grants-1993_05 |
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| ORD ID | ord-6cfe97d6e01c4c83a1905e2fa8b45e0c |
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| 出典メモ | uspto-grants-1993_05 |
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