Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Imidazole → N-(1-Octylnonyl)perylene-3,4-dicarboximide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Imidazole | HCID 795 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | 3,4,9,10-Perylenetetracarboxylic dianhydride | HCID 67191 | — |
| 반응물 | Heptadecan-9-amine | HCID 408570 | — |
| 반응물 | N-(2,5-Di-t-butylphenyl)perylene-3,4-dicarboximide | HCID 11081772 | — |
| 촉매 | Zinc acetate (USP) | HCID 2724192 | — |
| 생성물 | N-(1-Octylnonyl)perylene-3,4-dicarboximide | HCID 19033227 | — |
반응 단계
1.4 g (3.1 mmol) of perylene-3,4,9,10-tetracarboxylic dianhydride, 6.1 g of imidazole, 960 mg (3.7 mmol) of 9-aminoheptadecane (prepared according to DE-A 4,007,618), 150 mg (0.68 mmol) of zinc acetate dihydrate and 3.0 ml (170 mmol) of water are heated in an autoclave (100 ml) at 190° C. for 24 h. Workup is analogous to that used for preparing 2b. Yield 130 mg (7% by extractive recrystallization from methanol, such as described in Chem. Ber. 1985, 118, 4641) orange red crystals showing strong solid fluorescence, m.p. 143°-143.6° C. Rf (CHCl3 /silica gel)=0.94. UV (CHCl3): λmax (ε)=454 nm (sh, 17620), 485 (32530), 508 (29480). Fluorescence (CHCl3, exc. 485 nm): λmax (Irel)=572 (sh, 0.49), 536 (1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05650513 |
| 출처 데이터셋 | uspto-grants-1997_07 |
| ORD ID | ord-b148e3223a964806845bb601e8e248b0 |
| 출처 메모 | uspto-grants-1997_07 |