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Water → Trichloroacetaldehyde isopropyl alcoholate

HRID 27592
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 27592
S1C=[CH:4][CH:3]=[CH:2]1.[Cl:6][C:7]([Cl:11])([Cl:10])[CH:8]=[O:9].O>[Ti](Cl)(Cl)(Cl)Cl.CC(C)[O-].CC(C)[O-].CC(C)[O-].CC(C)[O-].[Ti+4].C(Cl)Cl>[CH:3]([O-:9])([CH3:4])[CH3:2].[Cl:6][C:7]([Cl:11])([Cl:10])[CH:8]=[O:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 3

HCID 962WaterHCID 6407ChloralHCID 8030Thiophene

Produkt 1

HCID 86737204Trichloroacetaldehyde isopropyl alcoholate

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 11026Titanium isopropoxideKatalysatorHCID 24193Titanium Tetrachloride
Katalysator
HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a solution of titanium tetrachloride in methylene chloride (1 molar concentration; 30 ml, 30 mmol), titanium tetraisopropoxide (4.26 g, 15 mmol) was added under an argon atmosphere with stirring and under water cooling. After 10 min., thiophene (2.52 g, 30 mmol) was added and then trichloroacetaldehyde (8.82 g, 60 mmol) was added dropwise during 10 min. with stirring and under ice-water cooling. After the addition was completed, stirring was continued for further 10 min., and then water and methylene chloride were added successively, and the organic layer was separated. The organic layer was washed with water and dried over anhydrous magnesium sulfate. The solution was filtered and, after removal of the solvent by distillation under a reduced pressure with an aspirator, the residue was distilled to form trichloroacetaldehyde isopropyl alcoholate initially and then 5.0 g of α-trichloromethyl-2-thiophenemethanol.

Aufarbeitung

  1. stirringwith stirring and under ice-water cooling
  2. additionAfter the addition
  3. stirringstirring
  4. waitwas continued for further 10 min.
  5. customthe organic layer was separated
  6. washThe organic layer was washed with water
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationThe solution was filtered
  9. customafter removal of the solvent
  10. distillationby distillation under a reduced pressure with an aspirator
  11. distillationthe residue was distilled

Quellen und Nachweise

ORD-Eintrag
ord-8e756189357d4ce1a1ba0509e6dac945
Quelldatensatz
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04221915

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