Reaktionsgleichung
[S:1]1[CH:5]=[CH:4][CH:3]=[CH:2]1.[Cl:6][C:7]([Cl:11])([Cl:10])[CH:8]=[O:9]>CCCCCCC>[Cl:6][C:7]([Cl:11])([Cl:10])[CH:8]([C:2]1[S:1][CH:5]=[CH:4][CH:3]=1)[OH:9]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Thiophene (4.2 g, 50 mmol) and trichloroacetaldehyde (7.35 g, 50 mmol) were dissolved in n-heptane (25 ml). The solution was heated under reflux for 3.5 hr. under a Soxleht apparatus in which Amberlyst 15 (4.2 g) had been placed. After cooling, the n-heptane solution was concentrated, and the residue was purified by distillation to give 2.32 g of α-trichloromethyl-2-thiophenemethanol boiling at 98°-100° C./1.0 mmHg.
Aufarbeitung
- temperatureThe solution was heated
- temperatureunder reflux for 3.5 hr
- temperatureAfter cooling
- concentrationthe n-heptane solution was concentrated
- distillationthe residue was purified by distillation
Quellen und Nachweise
- ORD-Eintrag
- ord-28b3a49b4b8d4b40a1cbd8ddf9546e9f
- Quelldatensatz
- uspto-grants-1980_09
- Patentnummer
- US04221915
Verknüpfte Notizen
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