Trifluoroacetic acid → (3RS,4R)-4-amino-2,2-dimethyl-hexan-3-ol
Reaktionsgleichung
[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
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a stirred solution of (3RS,4R)-2,2-dimethyl-4-(trityl-amino)-hexan-3-ol (0.57 g, 1 eq, 1.47 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 sting 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: 0.21 g (100%). (55% de 3S,4R: 45% de 3R,4R) 1H-NMR (d6-DMSO, 250 MHz): δ 0.84-0.99 (m, 3H, NH2CH(CH2CH3)CH(C(CH3)3)OH), 1.25-1.29 (m, 9H, NH2CH(CH2CH3)CH(C(CH3)3)OH), 1.20-1.72 (m, 2H, NH2CH(CH2CH3)CH(C(CH3)3)OH), 3.14 (m, 1H, NH2CH(CH2CH3)CH(C(CH3)3)OH), 3.39 (m, 1H, NH2CH(CH2CH3)CH(C(CH3)3)OH), 3.65 (m, 1H, NH2CH(CH2CH3)CH(C(CH3)3)OH), 7.43, 7.77+8.54 (3×bs, 2H, NH2CH(CH2CH3)CH(CH(CH3)2)OH).
Aufarbeitung
- customThe solvent was evaporated in vacuo
- customthe residue was precipitated from ether (3 mL) with hexane (20 mL)
- customto give a yellow oil
- customThe solvent was decanted from the oil
- washthe oil was washed with hexane (20 mL)
- customdried in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-799a21ef6db2487fbb089a438ce85fe0
- Quelldatensatz
- uspto-grants-2009_11
- Patentnummer
- US07612079B2
Notizen zur Reaktion
Wird geladen…