Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Quinone → 1,2,3,4,9,9-Hexachloro-1,4,4A,8A-tetrahydro-1,4-methanonaphthalene-5,8-dione
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Quinone | HCID 4650 | — |
| 반응물 | Hexachlorocyclopentadiene | HCID 6478 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 1,2,3,4,9,9-Hexachloro-1,4,4A,8A-tetrahydro-1,4-methanonaphthalene-5,8-dione | HCID 228947 | 64% |
반응 단계
A mixture of 54.6 g. (0.2 mole) of hexachlorocyclopentadiene, 21.6 g. (0.2 mole) of p-benzoquinone, and 10 ml. of toluene were placed in a 125 ml. round bottom flask and heated for three hours so that the toluene refluxed gently. At the end of this period the reaction mixture suddenly solidified completely, indicating completion of the reaction. The crude product was bright yellow. The damp material was transferred to a Buchner funnel, rinsed with absolute ethanol, dried on the funnel, and crystallized from ethanol. 49 g. of bright yellow dense crystals were obtained, m.p. 189°-193° C. (reported 188° C.). The yield was 64%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04174457 |
| 출처 데이터셋 | uspto-grants-1979_11 |
| ORD ID | ord-007537d4767341d98b1cc83e9e5903de |
| 출처 메모 | uspto-grants-1979_11 |