Acetic Acid → 4-[(S)-1-(4-Bromo-phenyl)-ethylamino]-1-methoxy-2-phenyl-butan-2-ol

HRID 80961

Reaktionsgleichung

Reaktionsgleichung von HRID 80961
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C@@H:8]([NH2:10])[CH3:9])=[CH:4][CH:3]=1.C(O)(=O)C.[OH:15][C:16]([C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)([CH2:20][O:21][CH3:22])[CH2:17][CH:18]=O>O1CCCC1>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C@@H:8]([NH:10][CH2:18][CH2:17][C:16]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)([OH:15])[CH2:20][O:21][CH3:22])[CH3:9])=[CH:4][CH:3]=1

Komponenten

5

Edukt 3

HCID 176Acetic AcidHCID 852999(alphaS)-4-Bromo-alpha-methylbenzenemethanamineHCID 596356773-Hydroxy-4-methoxy-3-phenyl-butyraldehyde

Produkt 1

HCID 596357994-[(S)-1-(4-Bromo-phenyl)-ethylamino]-1-methoxy-2-phenyl-butan-2-ol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

(S)-1-(4-Bromo-phenyl)-ethylamine (0.93 g), NaHB(O2CH3)3 (0.98 g), and acetic acid (0.27 mL) were added in the given order to a solution of 3-hydroxy-4-methoxy-3-phenyl-butyraldehyde (0.90 g) in tetrahydrofuran (20 mL) at ca. 10-15° C. The cooling bath was removed and the mixture was stirred at room temperature for 2 h. Then, water (50 mL) and 1 M aqueous NaOH solution (20 mL) were added and the resulting mixture was stirred for another 30 min. The mixture was extracted with ethyl acetate and the combined extracts were washed with water and brine. After drying (MgSO4), the solvent was removed to give the title compound which was used without further purification.

Aufarbeitung

  1. customThe cooling bath was removed
  2. additionThen, water (50 mL) and 1 M aqueous NaOH solution (20 mL) were added
  3. stirringthe resulting mixture was stirred for another 30 min
  4. extractionThe mixture was extracted with ethyl acetate
  5. washthe combined extracts were washed with water and brine
  6. dry with materialAfter drying (MgSO4)
  7. customthe solvent was removed

Quellen und Nachweise

ORD-Eintrag
ord-eb07a31fdd0042a4986199d4d942dbe5
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08846668B2

Verknüpfte Notizen

Wird geladen…