Potassium Carbonate → [4-Chloro-2-(cyclopropylmethoxy)phenyl]methanol

HRID 878613

Reaktionsgleichung

Reaktionsgleichung von HRID 878613
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:9][OH:10])=[C:6]([OH:8])[CH:7]=1.Br[CH:12]([CH:14]1[CH2:16][CH2:15]1)O.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:9][OH:10])=[C:6]([O:8][CH2:12][CH:14]2[CH2:16][CH2:15]2)[CH:7]=1

Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 3271485-Chloro-2-(hydroxymethyl)phenolHCID 53647370HCID 53647370, Verbindung

Produkt 1

HCID 86725580[4-Chloro-2-(cyclopropylmethoxy)phenyl]methanolAusbeute 13,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

Charged 5-chloro-2-(hydroxymethyl)phenol (616 mg, 3.88 mmol, PREPARATION 7), bromocyclopropylmethanol (525 mg, 3.88 mmol), K2CO3 (1.07 g, 7.77 mmol) and DMF (6 mL) to a flask, purged with nitrogen and heated to 80° C. overnight. Poured into ice water, and extracted with ethyl acetate twice, and washed the organic phase with water twice, brine and dried with anhydrous Na2SO4, removed the solvent for silica gel chromatograph to give 108 mg of the title compound (13%). 1H NMR (400 MHz, CDCl3): δ 0.33-0.37 (2H, m), 0.63-0.68 (2H, m), 1.26-1.28 (1H, m), 3.84 (2H, d, J=7.2 Hz), 4.67 (2H, s), 4.86 (1H, s), 6.84 (1H, d, J=1.2 Hz), 6.91 (1H, dd, J=2.0 Hz, 8.0 Hz), 7.19 (1H, d, J=7.6 Hz).

Aufarbeitung

  1. custompurged with nitrogen
  2. additionPoured into ice water
  3. extractionextracted with ethyl acetate twice
  4. washwashed the organic phase with water twice
  5. dry with materialbrine and dried with anhydrous Na2SO4
  6. customremoved the solvent for silica gel chromatograph

Quellen und Nachweise

ORD-Eintrag
ord-2cb3fb8b1ae341909b1f78d7235fbf1b
Quelldatensatz
uspto-grants-2015_03
Patentnummer
US08987461B2

Verknüpfte Notizen

Wird geladen…