Phosphorus oxychloride → 2-Chloro-6-(2,6-diethyl-phenyl)-4-ethyl-nicotinic acid methyl ester

HRID 1392631Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1392631
[CH3:1][O:2][C:3](=[O:23])[C:4]1[C:9]([CH2:10][CH3:11])=[CH:8][C:7]([C:12]2[C:17]([CH2:18][CH3:19])=[CH:16][CH:15]=[CH:14][C:13]=2[CH2:20][CH3:21])=[N+:6]([O-])[CH:5]=1.O=P(Cl)(Cl)[Cl:26]>>[CH3:1][O:2][C:3](=[O:23])[C:4]1[C:9]([CH2:10][CH3:11])=[CH:8][C:7]([C:12]2[C:17]([CH2:18][CH3:19])=[CH:16][CH:15]=[CH:14][C:13]=2[CH2:20][CH3:21])=[N:6][C:5]=1[Cl:26]

Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 669936046-(2,6-diethyl-phenyl)-4-ethyl-nicotinic acid methyl ester N-oxide

Produkt 1

HCID 596782342-Chloro-6-(2,6-diethyl-phenyl)-4-ethyl-nicotinic acid methyl ester

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

A mixture of 6-(2,6-diethyl-phenyl)-4-ethyl-nicotinic acid methyl ester N-oxide (1.7 g) and POCl3 (10 mL) is heated at 80° C. for 2 hours. The volatile material is removed in vacuo. Ice water and ether is added to the residue. The organic layer is separated and the aqueous layer is extracted with ether. The combined extract is washed with brine, dried, and concentrated to give 2-chloro-6-(2,6-diethyl-phenyl)-4-ethyl-nicotinic acid methyl ester. 1H NMR (CDCl3) 7.26 (t, 1H), 7.12 (d, 3H), 4.02 (s, 3H), 2.69 (q, 2H), 2.32 (m, 4H), 1.25 (t, 3H), 1.07 (t, 6H).

Aufarbeitung

  1. customThe volatile material is removed in vacuo
  2. additionIce water and ether is added to the residue
  3. customThe organic layer is separated
  4. extractionthe aqueous layer is extracted with ether
  5. extractionThe combined extract
  6. washis washed with brine
  7. customdried
  8. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-6dbcf6a3c01a4f22aedad75b4265e831
Quelldatensatz
uspto-grants-2008_03
Patentnummer
US07342115B2

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