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Phosphorus oxychloride → 6-[(4-Formylphenyl)(methyl)amino]hexyl acetate

HRID 1199286
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1199286
P(Cl)(Cl)(Cl)=O.[C:6]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][N:16]([CH3:23])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)(=[O:8])[CH3:7].[C:24]([O-])(=[O:26])C.[Na+]>CN(C)C=O>[C:6]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][N:16]([CH3:23])[C:17]1[CH:18]=[CH:19][C:20]([CH:24]=[O:26])=[CH:21][CH:22]=1)(=[O:8])[CH3:7]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 24813Phosphorus oxychlorideHCID 517045Sodium AcetateHCID 19697246N-(6-Acetoxyhexyl)-N-methylaniline

Produkt 1

HCID 152539796-[(4-Formylphenyl)(methyl)amino]hexyl acetateAusbeute 73 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

Phosphorous oxychloride (145 g, 0.95 mol) was added dropwise at 5° C. to 280 mL of stirred N,N-dimethylformamide (DMF), and the mixture was stirred at 5° C. for 2 hours. N-(6-Acetoxyhexyl)-N-methylaniline (Example 2, 230 g, 0.93 mol) was added slowly, and the reaction mixture was heated at 90° C. for 3 hours. After cooling, the solution was poured onto 500 g of ice and the resulting mixture was neutralized to pH 5 with sodium acetate. The mixture was extracted with dichloromethane (4×200 mL), the combined extracts were dried (MgSO4), and the solvent was removed at reduced pressure. The brown residue was distilled in vacuo to provide 186 g (73%) of a yellow oil, bp 195° C. (0.15 mm).

Aufarbeitung

  1. temperaturethe reaction mixture was heated at 90° C. for 3 hours
  2. temperatureAfter cooling
  3. extractionThe mixture was extracted with dichloromethane (4×200 mL)
  4. dry with materialthe combined extracts were dried (MgSO4)
  5. customthe solvent was removed at reduced pressure
  6. distillationThe brown residue was distilled in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-3cf62ed54efa4958b9782ef1499031b0
Quelldatensatz
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04900127

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