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2-(Methylamino)ethanol → HCID 57663183, Verbindung

HRID 548653
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 548653
CCN(C(C)C)C(C)C.F[C:11]1[C:19]([F:20])=[C:18]([F:21])[CH:17]=[CH:16][C:12]=1[C:13](Cl)=[O:14].[CH3:22][NH:23][CH2:24][CH2:25][OH:26].[H-].[Na+]>C(Cl)Cl.CO.O>[F:21][C:18]1[CH:17]=[CH:16][C:12]2[C:13](=[O:14])[N:23]([CH3:22])[CH2:24][CH2:25][O:26][C:11]=2[C:19]=1[F:20]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 80162-(Methylamino)ethanolHCID 24758Sodium hydrideHCID 81531DiisopropylethylamineHCID 27340222,3,4-Trifluorobenzoyl chloride

Produkt 1

HCID 57663183HCID 57663183, VerbindungAusbeute 21,1 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 887
Methanol
Lösungsmittel
HCID 962WaterLösungsmittel
HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

DIPEA (0.68 mL, 3.9 mmol) was added to a solution of 2,3,4-trifluorobenzoyl chloride (500 mg, 2.6 mmol) in DCM (5 mL) followed by the addition of N-methylethanolamine (0.31 mL, 3.9 mmol). The mixture was stirred for 20 hours. The solution was diluted with methanol (10 mL) and passed through an ISOLUTE® SCX-2 SPE column. The solution was evaporated. The residue was dissolved in DMF and sodium hydride (60% dispersion in mineral oil, 0.11 g, 2.7 mmol) was added portionwise over 5 minutes. The resulting mixture was stirred for 20 hours. Water (100 mL) was added dropwise and the mixture was extracted with ether (3×200 mL). Combined ethereal extracts were dried (MgSO4) and evaporated. The residue was purified by column chromatography (eluting with 1:1 ethyl acetate:isohexane to neat ethyl acetate) to afford the title compound (117 mg, 20%) as a colourless solid.

Aufarbeitung

  1. customThe solution was evaporated
  2. dissolutionThe residue was dissolved in DMF
  3. stirringThe resulting mixture was stirred for 20 hours
  4. extractionthe mixture was extracted with ether (3×200 mL)
  5. dry with materialwere dried (MgSO4)
  6. customevaporated
  7. customThe residue was purified by column chromatography (eluting with 1:1 ethyl acetate:isohexane to neat ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-b45d8d43704e422eb09e2c1f9e231196
Quelldatensatz
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07943607B2

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