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HRID 369667Erstellt: 24. Oktober 2026
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/de/reaction/369667
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,1,1-Trichloro-2,2,2-trifluoroethane | HCID 9635 | — |
| Edukt | 4-(2,6-Dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde | HCID 53826908 | — |
| Katalysator | Zinc | HCID 23994 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 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% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06140274 |
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| Quelldatensatz | uspto-grants-2000_10 |
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| ORD ID | ord-0618dde99335441b96a472b8e46bca52 |
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| Quellennotiz | uspto-grants-2000_10 |
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