Water → Trichloroacetaldehyde isopropyl alcoholate

HRID 27592

Reaction equation

HRID 27592 reaction equation
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]

Participants

7

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-8e756189357d4ce1a1ba0509e6dac945
Source dataset
uspto-grants-1980_09
Patent number
US04221915

Linked notes

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