Water → Diethyl 2,4-diisopropoxy-6-(trifluoromethyl)-3,5-pyridinedicarboxylate

HRID 64570Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 64570
[Li+].CC([N-]C(C)C)C.[CH:9]([O:12][C:13]1[CH:18]=[C:17]([O:19][CH:20]([CH3:22])[CH3:21])[N:16]=[C:15]([C:23]([F:26])([F:25])[F:24])[C:14]=1[C:27]([O:29][CH2:30][CH3:31])=[O:28])([CH3:11])[CH3:10].Cl[C:33]([O:35][CH2:36][CH3:37])=[O:34].O>COCCOC>[CH:20]([O:19][C:17]1[C:18]([C:33]([O:35][CH2:36][CH3:37])=[O:34])=[C:13]([O:12][CH:9]([CH3:10])[CH3:11])[C:14]([C:27]([O:29][CH2:30][CH3:31])=[O:28])=[C:15]([C:23]([F:24])([F:26])[F:25])[N:16]=1)([CH3:22])[CH3:21]

Komponenten

6

Versuchsvorschrift

To a -78° C. solution of 0.021 mol of LDA in DME (30 ml) was added a solution of 4.65 g (0.014 mol) of product of Example 6 in 20 ml of DME. The resulting solution was stirred for 10 minutes and treated with 2.7 ml (0.035 mol) of ethyl chloroformate. After stirring at -78° C. for 30 minutes the reaction mixture was warmed to room temperature in 30 minutes and poured into 50 ml of water. The mixture was extracted with ether. The ether extract was washed with 10% K2CO3, dried over CaSO4 and concentrated. The residue was first kugelrohr distilled at 0.15 torr (pot temperature 55° C.) to remove low boiling material (1.08 g), then distilled at 164°-173° C. (0.15 torr) to give 1.95 g (34.5%) of product as an oil.

Aufarbeitung

  1. stirringAfter stirring at -78° C. for 30 minutes the reaction mixture
  2. extractionThe mixture was extracted with ether
  3. extractionThe ether extract
  4. washwas washed with 10% K2CO3
  5. dry with materialdried over CaSO4
  6. concentrationconcentrated
  7. distillationdistilled at 0.15 torr (pot temperature 55° C.)
  8. customto remove low boiling material (1.08 g)
  9. distillationdistilled at 164°-173° C. (0.15 torr)

Quellen und Nachweise

ORD-Eintrag
ord-ea6929a300ef40f88e9a6aec6f60e869
Quelldatensatz
uspto-grants-1986_09
Patentnummer
US04609399

Notizen zur Reaktion

Wird geladen…