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Acetic Anhydride → 2-Hydroxymethyl-3-methyl-4-(2,2,3,3,3-pentafluoropropoxy)pyridine

HRID 353004
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 353004
[CH3:1][C:2]1[C:7]([CH3:8])=[C:6]([O:9][CH2:10][C:11]([F:17])([F:16])[C:12]([F:15])([F:14])[F:13])[CH:5]=[CH:4][N+:3]=1[O-].C(OC(=O)C)(=[O:21])C>S(=O)(=O)(O)O>[OH:21][CH2:1][C:2]1[C:7]([CH3:8])=[C:6]([O:9][CH2:10][C:11]([F:17])([F:16])[C:12]([F:15])([F:14])[F:13])[CH:5]=[CH:4][N:3]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 7918Acetic AnhydrideHCID 136547942,3-Dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)pyridine-1-oxide

Produkt 1

HCID 136547662-Hydroxymethyl-3-methyl-4-(2,2,3,3,3-pentafluoropropoxy)pyridine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1118Sulfuric AcidKatalysator

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

Concentrated sulfuric acid (2 drops) was added to a solution or 2,3-dimethyl-4-(2,2,3,3,3-pentafluoropropoxy)-pyridine-1-oxide (2.5 g) in acetic anhydride (8 ml) and the mixture was stirred at 110° C. for 2 hours and then concentrated. The residue was dissolved in methanol (30 ml), 2 N aqueous sodium hydroxide (20 ml) was added, and the mixture was stirred at room temperature for 2 hours. After concentration, water was added to the residue and the mixture was extracted with ethyl acetate. The extract was dried over magnesium sulfate, the solvent was then distilled off, and the residue was applied to a silica gel (50 g) column. Elution with chloroform-methanol (10:1) and recrystallization from isopropyl ether gave 1.6 g of 2-hydroxymethyl-3-methyl-4-(2,2,3,3,3-pentafluoropropoxy)-pyridine as a brown oil.

Aufarbeitung

  1. concentrationconcentrated
  2. dissolutionThe residue was dissolved in methanol (30 ml)
  3. addition2 N aqueous sodium hydroxide (20 ml) was added
  4. stirringthe mixture was stirred at room temperature for 2 hours
  5. concentrationAfter concentration, water
  6. additionwas added to the residue
  7. extractionthe mixture was extracted with ethyl acetate
  8. dry with materialThe extract was dried over magnesium sulfate
  9. distillationthe solvent was then distilled off
  10. washElution
  11. customwith chloroform-methanol (10:1) and recrystallization from isopropyl ether

Quellen und Nachweise

ORD-Eintrag
ord-79760a2e2d634cfab19947abbde3edd7
Quelldatensatz
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06749864B2

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