Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 369667생성일: 2026년 10월 24일
1,1,1-Trichloro-2,2,2-trifluoroethane → 3,5-Dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3,3-dichloro-4,4,4-trifluoro-2-hydroxybutyloxy)butyloxy)benzene
https://huagongshe.com/ko/reaction/369667
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1,1,1-Trichloro-2,2,2-trifluoroethane | HCID 9635 | — |
| 반응물 | 4-(2,6-Dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde | HCID 53826908 | — |
| 촉매 | Zinc | HCID 23994 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3,5-Dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3,3-dichloro-4,4,4-trifluoro-2-hydroxybutyloxy)butyloxy)benzene | HCID 23282413 | 63.4% |
반응 단계
To a mixture of 2.01 g of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde, 1.31 g of zinc dust and 10 ml of N,N-dimethylformamide was added 4.12 g of 1,1,1-trichlorotrifluoroethane. After stirring at room temperature for 1.5 hours, the reaction mixture was filtered. The filtrate was poured into 20 ml of diluted hydrochloric acid and extracted twice with 50 ml of ethyl acetate. The ethyl acetate layers were combined, washed with water, dried over magnesium sulfate and then evaporated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 1.76 g of 3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3,3-dichloro-4,4,4-trifluoro-2-hydroxybutyloxy)butyloxy)benzene (yield, 63%), nD24.2 1.5188.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06140274 |
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| 출처 데이터셋 | uspto-grants-2000_10 |
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| ORD ID | ord-0618dde99335441b96a472b8e46bca52 |
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| 출처 메모 | uspto-grants-2000_10 |
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