Reaktion #2286303

ord-dd4841b692e048c9ab4c4a6255394cc5

Reaktionsgleichung

CC(C)c1cc(Oc2c(Cl)cc(CCO)cc2Cl)nnc1Cl
2-[3,5-dichloro-4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-phenyl]-ethanol
CC(C)c1cc(Oc2c(Cl)cc(CCO)cc2Cl)nnc1Cl
2-[3,5-Dichloro-4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-phenyl]-ethanol
CC(=O)[O-].[Na+]
sodium acetate
CC(=O)O
acetic acid
CC(=O)OCCc1cc(Cl)c(Oc2cc(C(C)C)c(=O)[nH]n2)c(Cl)c1
acetic acid 2-[3,5-dichloro-4-(5-isopropyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-ethyl ester
Ausbeute 100.0%
CC(=O)OCCc1cc(Cl)c(Oc2cc(C(C)C)c(=O)[nH]n2)c(Cl)c1
Acetic acid 2-[3,5-dichloro-4-(5-isopropyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-ethyl ester
Ausbeute 100.0%

Reaktionsbedingungen

Temperatur
114°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturAt this time, the reaction mixture was cooled to room temperature
  2. 2
    Einengenwas concentrated under vacuum
  3. 3
    workup.ADDITIONThe resulting residue was diluted with methylene chloride (25 mL)
  4. 4
    Waschenwas washed with water (10 mL)
  5. 5
    SonstigeThe organic layer was separated
  6. 6
    Waschenwas washed with a saturated aqueous sodium bicarbonate solution (10 mL)
  7. 7
    Extraktionextracted with methylene chloride (10 mL)
  8. 8
    Trocknendried with sodium sulfate
  9. 9
    Filtrationfiltered
  10. 10
    Einengenconcentrated
  11. 11
    Sonstigedried under high vacuum overnight

Vorschrift

A solution of 2-[3,5-dichloro-4-(6-chloro-5-isopropyl-pyridazin-3-yloxy)-phenyl]-ethanol (17) (500 mg, 1.38 mmol) in glacial acetic acid (5 mL) was treated with sodium acetate (230 mg, 2.8 mmol) and heated to 114° C. for 24 h. At this time, the reaction mixture was cooled to room temperature and was concentrated under vacuum. The resulting residue was diluted with methylene chloride (25 mL) and was washed with water (10 mL). The organic layer was separated and was washed with a saturated aqueous sodium bicarbonate solution (10 mL). The waters layers were combined and extracted with methylene chloride (10 mL). The organic layers were combined and dried with sodium sulfate, filtered, concentrated and dried under high vacuum overnight to afford acetic acid 2-[3,5-dichloro-4-(5-isopropyl-6-oxo-1,6-dihydro-pyridazin-3-yloxy)-phenyl]-ethyl ester (34) (531 mg, 100%) as a white solid; LRMS for C17H18Cl2N2O4 (M+) m/z=385 Molecular Weight=385.2500; Exact Mass=384.0644

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE046024E1uspto-grants-2016_06