Hydrochloric Acid → 1-Amino-3-(cholestan-3-yloxy)-propane

HRID 74861

Reaktionsgleichung

Reaktionsgleichung von HRID 74861
[CH3:1][CH:2]([CH2:4][CH2:5][CH2:6][C@H:7]([C@@H:9]1[C@:26]2([CH3:27])[C@H:12]([C@H:13]3[C@H:23]([CH2:24][CH2:25]2)[C@:21]2([CH3:22])[CH:16]([CH2:17][CH:18]([O:28][CH2:29][CH2:30][C:31]#[N:32])[CH2:19][CH2:20]2)[CH2:15][CH2:14]3)[CH2:11][CH2:10]1)[CH3:8])[CH3:3].C(Cl)(Cl)Cl.CCO.Cl>C1(C)C=CC=CC=1.O.[Pt]=O>[NH2:32][CH2:31][CH2:30][CH2:29][O:28][CH:18]1[CH2:19][CH2:20][C@@:21]2([CH3:22])[CH:16]([CH2:15][CH2:14][C@@H:13]3[C@@H:23]2[CH2:24][CH2:25][C@@:26]2([CH3:27])[C@H:12]3[CH2:11][CH2:10][C@@H:9]2[C@H:7]([CH3:8])[CH2:6][CH2:5][CH2:4][CH:2]([CH3:1])[CH3:3])[CH2:17]1

Komponenten

7

Versuchsvorschrift

3-(Cholestan-3-yloxy)propanenitrile 135 (442 mg, 1 mmol) was taken up in a mixture of toluene (1 mL), chloroform (1.5 mL), EtOH (1 mL) and conc. HCl (200 μL). Platinum oxide hydrate (46 mg) was added. The mixture was stirred under hydrogen (80 psi) at room temperature for 48 hours. The solvent was evaporated and the residue taken up with DCM (40 mL) and NaHCO3 (sat.) (40 mL). The organic phase was separated and washed with NaHCO3 (sat.) (30 mL), followed by brine (20 mL), before being dried (Na2SO4) and the solvent evaporated to yield the white foam product which was reacted on without further purification or characterization.

Aufarbeitung

  1. customThe solvent was evaporated
  2. customThe organic phase was separated
  3. washwashed with NaHCO3 (sat.) (30 mL)
  4. dry with materialbefore being dried (Na2SO4)
  5. customthe solvent evaporated
  6. customto yield the white foam product which
  7. customwas reacted on without further purification or characterization

Quellen und Nachweise

ORD-Eintrag
ord-8d1a18749b7445aa82209e3c4e390308
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08828952B2

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