Trifluoroacetic acid → (3RS,4S)-4-amino-2,2-dimethyl-hexan-3-ol

HRID 1432410Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1432410
[CH3:1][C:2]([CH3:29])([CH:4]([OH:28])[C@@H:5]([NH:8]C(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[CH2:6][CH3:7])[CH3:3].FC(F)(F)C(O)=O>C(Cl)Cl>[NH2:8][C@@H:5]([CH2:6][CH3:7])[CH:4]([OH:28])[C:2]([CH3:29])([CH3:3])[CH3:1]

Komponenten

4

Versuchsvorschrift

To a stirred solution of (3RS,4S)-2,2-dimethyl-4-(trityl-amino)-hexan-3-ol (0.47 g, 1 eq, 1.21 mmol) in DCM (10 mL) under an argon atmosphere at room temperature, was added trifluoroacetic acid (5 mL) dropwise, and the solution was stirred at this temperature for 1 h. The solvent was evaporated in vacuo, the residue was precipitated from ether (3 mL) with hexane (20 mL) with stirring to give a yellow oil. The solvent was decanted from the oil, and the oil was washed with hexane (20 mL) and dried in vacuo to afford the title compound as a light yellow oil; Yield: 0.18 g (99%). (53% de 3R,4S: 47% de 3S,4S). 1H-NMR (d6-DMSO, 250 MHz): δ 0.86-0.99 (m, 3H, NH2CH(CH2CH3)CH(C(CH3)3)OH), 1.25-1.30 (m, 9H, NH2CH(CH2CH3)CH(C(CH3)OH), 1.20-1.67 (m, 2H, NH2CH(CH2CH3)CH(C(CH3)3)OH), 3.14 (m, 1H, NH2CH(CH2CH3)CH(C(CH3)3)OH), 3.38 (m, 1H, NH2CH(CH2CH3)CH(C(CH3)3)OH), 3.64 (m, 1H, NH2CH(CH2CH3)CH(C(CH3)3)OH), 7.41, 7.73+8.44 (3×bs, 2H, NH2CH(CH2CH3)CH(CH(CH3)2)OH).

Aufarbeitung

  1. customThe solvent was evaporated in vacuo
  2. customthe residue was precipitated from ether (3 mL) with hexane (20 mL)
  3. stirringwith stirring
  4. customto give a yellow oil
  5. customThe solvent was decanted from the oil
  6. washthe oil was washed with hexane (20 mL)
  7. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-6d2993b829b942a9b5589eb4dbdad5ac
Quelldatensatz
uspto-grants-2009_11
Patentnummer
US07612079B2

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