Trimethyl orthoformate → 3-Chloro-2-(4-chloro-3-dimethoxymethylphenyl)-5-trifluoromethylpyridine

HRID 1957260Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1957260
[CH:1](OC)([O:4][CH3:5])[O:2][CH3:3].O.[O-2].[O-2].[O-2].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.[Al+3].[Al+3].[Cl:26][C:27]1[C:28]([C:37]2[CH:42]=[CH:41][C:40]([Cl:43])=[C:39](C=O)[CH:38]=2)=[N:29][CH:30]=[C:31]([C:33]([F:36])([F:35])[F:34])[CH:32]=1>ClCCl>[Cl:26][C:27]1[C:28]([C:37]2[CH:42]=[CH:41][C:40]([Cl:43])=[C:39]([CH:1]([O:4][CH3:5])[O:2][CH3:3])[CH:38]=2)=[N:29][CH:30]=[C:31]([C:33]([F:35])([F:36])[F:34])[CH:32]=1

Komponenten

5

Edukt 3

HCID 9005Trimethyl orthoformateHCID 186929322-Chloro-5-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]benzaldehydeHCID 71586775Bentonite

Produkt 1

HCID 190687453-Chloro-2-(4-chloro-3-dimethoxymethylphenyl)-5-trifluoromethylpyridine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

50 ml of trimethyl orthoformate were added to 40.0 g of montmorillonite K-10 in 250 ml of anhydrous dichloromethane, after which a solution of 20.0 g of 3-chloro-2-(4-chloro-3-formylphenyl)-5-trifluoromethylpyridine in 50 ml of dichloromethane was added dropwise while stirring and cooling in ice. After stirring at 23° C. for 20 hours, the clay was removed and thoroughly washed with dichloromethane. The dichloromethane phase was concentrated. The residue was purified by chromatography on silica gel with cyclohexane/ethyl acetate (10:1). Yield: 22.1 g (96%) of a colorless oil.

Aufarbeitung

  1. temperaturecooling in ice
  2. stirringAfter stirring at 23° C. for 20 hours
  3. customthe clay was removed
  4. washthoroughly washed with dichloromethane
  5. concentrationThe dichloromethane phase was concentrated
  6. customThe residue was purified by chromatography on silica gel with cyclohexane/ethyl acetate (10:1)

Quellen und Nachweise

ORD-Eintrag
ord-0ffccac45b144b839e75b0fdf07c86d6
Quelldatensatz
uspto-grants-1998_07
Patentnummer
US05783522

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