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Ammonium Chloride → 2-[(2,4-Difluorophenyl)(hydroxy)methyl]cyclopropanecarbonitrile

HRID 561486
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 561486
[BH4-].[Na+].[F:3][C:4]1[CH:16]=[C:15]([F:17])[CH:14]=[CH:13][C:5]=1[C:6]([CH:8]1[CH2:10][CH:9]1[C:11]#[N:12])=[O:7].[Cl-].[NH4+]>C(O)C.C(OCC)(=O)C>[F:3][C:4]1[CH:16]=[C:15]([F:17])[CH:14]=[CH:13][C:5]=1[CH:6]([OH:7])[CH:8]1[CH2:10][CH:9]1[C:11]#[N:12]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 25517Ammonium ChlorideHCID 4311764Sodium borohydrideHCID 583925512-(2,4-Difluorobenzoyl)cyclopropanecarbonitrile

Produkt 1

HCID 583924722-[(2,4-Difluorophenyl)(hydroxy)methyl]cyclopropanecarbonitrile

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittel
HCID 8857
Ethyl Acetate
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

342 mg (9.03 mmol) of sodium borohydride were added to 1.70 g (8.21 mmol) of the compound from Example 123A in 35 ml of ethanol and 15 ml of ethyl acetate under argon, and the mixture was stirred at 40° C. for 1 h. The reaction mixture was added to saturated aqueous ammonium chloride solution and ethyl acetate, the phases were separated, the aqueous phase was extracted twice with ethyl acetate, and the combined organic phases were dried over magnesium sulfate, filtered and concentrated. The crude product was purified by flash chromatography on silica gel (mobile phase: toluene/ethyl acetate 9/1) to result in 1.50 g (87% of theory) of a mixture of the diastereomers of the title compound.

Aufarbeitung

  1. customthe phases were separated
  2. extractionthe aqueous phase was extracted twice with ethyl acetate
  3. dry with materialthe combined organic phases were dried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude product was purified by flash chromatography on silica gel (mobile phase: toluene/ethyl acetate 9/1)

Quellen und Nachweise

ORD-Eintrag
ord-80b5b8dcd3ad4307a8e5f123e6e73631
Quelldatensatz
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08063234B2

Notizen zur Reaktion

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