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Ammonium Hydroxide → 4,4-Difluorocyclohexanecarboxamide

HRID 1049324
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1049324
[F:1][C:2]1([F:11])[CH2:7][CH2:6][CH:5]([C:8](O)=[O:9])[CH2:4][CH2:3]1.C(Cl)(=O)C(Cl)=O.[NH4+:18].[OH-]>C(Cl)Cl.CN(C=O)C.C1COCC1.[Cl-].[Na+].O>[F:1][C:2]1([F:11])[CH2:7][CH2:6][CH:5]([C:8]([NH2:18])=[O:9])[CH2:4][CH2:3]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 3

HCID 14923Ammonium HydroxideHCID 65578Oxalyl chlorideHCID 27791364,4-Difluorocyclohexanecarboxylic acid

Produkt 1

HCID 469422314,4-DifluorocyclohexanecarboxamideAusbeute 77,4 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 6228DimethylformamideKatalysator
HCID 6344
Dichloromethane
Lösungsmittel
HCID 8028TetrahydrofuranLösungsmittel
HCID 57417360Sodium chloride; waterLösungsmittel

Versuchsvorschrift

A solution of 4,4-difluorocyclohexanecarboxylic acid (0.217 g, 1.322 mmol) in DCM (4 mL) was treated with oxalyl chloride (0.174 mL, 1.983 mmol) followed by catalytic DMF (1 drop) and the mixture stirred at RT for 1.5 h. The mixture was concentrated to dryness, co-evaporated with DCM (1×) and the resulting residue dissolved in THF (2 mL), added to a stirring solution of NH4OH (˜14M, 2 mL, 28.0 mmol) in THF (2 mL) and stirred for 30 minutes. The mixture was diluted with brine, extracted with EtOAc (3×) and the combined organics were dried over MgSO4 and concentrated to dryness to afford 4,4-difluorocyclohexanecarboxamide (167 mg, 77%) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ 7.28 (s, 1H), 6.79 (s, 1H), 2.20 (m, 1H), 2.00 (m, 2H), 1.86-1.67 (m, 4H), 1.57 (m, 2H).

Aufarbeitung

  1. concentrationThe mixture was concentrated to dryness, co-evaporated with DCM (1×)
  2. dissolutionthe resulting residue dissolved in THF (2 mL)
  3. stirringstirred for 30 minutes
  4. extractionextracted with EtOAc (3×)
  5. dry with materialthe combined organics were dried over MgSO4
  6. concentrationconcentrated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-e481285497f24033a19702b19b09a06e
Quelldatensatz
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09382228B2

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