Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247785생성일: 2026년 10월 26일
Benzoic acid, 4-((1-oxodecyl)oxy)- → 4-(1,1,1-Trifluoro-2-decyloxycarbonyl)phenyl 4-n-decanoyloxybenzoate
https://huagongshe.com/reaction/247785
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzoic acid, 4-((1-oxodecyl)oxy)- | HCID 3608562 | — |
| 반응물 | 1,1,1-Trifluoro-2-decyl 4-hydroxybenzoate | HCID 14745754 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-(1,1,1-Trifluoro-2-decyloxycarbonyl)phenyl 4-n-decanoyloxybenzoate | HCID 19013920 | — |
반응 단계
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
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05207947 |
|---|
| 출처 데이터셋 | uspto-grants-1993_05 |
|---|
| ORD ID | ord-6cfe97d6e01c4c83a1905e2fa8b45e0c |
|---|
| 출처 메모 | uspto-grants-1993_05 |
|---|