Acetone Cyanohydrin → 5,6-Dihydro-4-hydroxy-3-[(2-isopropylphenyl)methyl]-6-(3-methylbutyl)-6-phenyl-2H-pyran-2-one

HRID 357887Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 357887
[OH:1][C:2]1[CH2:7][C:6]([CH2:14][CH2:15][CH:16]([CH3:18])[CH3:17])([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[O:5][C:4](=[O:19])[CH:3]=1.CCN(CC)CC.[CH:27]([C:30]1[CH:38]=[CH:37][CH:36]=[CH:35][C:31]=1[C:32](Cl)=O)([CH3:29])[CH3:28].CC(C)(O)C#N.C([BH3-])#N.[Na+]>C(O)(=O)C.C(#N)C.C(Cl)Cl>[OH:1][C:2]1[CH2:7][C:6]([CH2:14][CH2:15][CH:16]([CH3:17])[CH3:18])([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[O:5][C:4](=[O:19])[C:3]=1[CH2:32][C:31]1[CH:35]=[CH:36][CH:37]=[CH:38][C:30]=1[CH:27]([CH3:29])[CH3:28]

Komponenten

9

Versuchsvorschrift

The title compound was prepared as described in General Method 8 using the following: 5,6-dihydro-4-hydroxy-6-(3-methylbutyl)-6-phenyl-2H-pyran-2-one (0.300 g, 1.15 mmol), Et3N (0.17 mL, 1.2 mmol), 2-isopropylbenzoyl chloride (1.15 mmol), CH2Cl2 (4.0 mL), acetonitrile (4.0 mL), acetone cyanohydrin (0.05 mL, 0.5 mmol), Et3N (0.35 mL, 2.5 mmol), glacial acetic acid (5.0 mL), sodium cyanoborohydride (0.50 g, 8.1 mmol). Purification was achieved by submitting the final residue to column chromatograpy (SiO2, 100% CH2Cl2) to provide a solid (0.118 g, 124°-126° C.) . 1H NMR (400 MHz, DMSO-d6) δ 10.855 (bs, 1 H), 7.395-7.306 (m, 5 H), 7.115 (dd, 1 H, J=1 Hz, J=7.5 Hz), 6.991 (t, 1 H, J=7 Hz), 6.622 (td, I H, J=1 Hz, J=7 Hz), 6.123 (d, 1 H, J=7 Hz), 3.422 (s, 2 H), 3.210-3.102 (m, 3 H), 1.975-1.871 (m, 2 H), 1.437-1.371 (m, 1 H), 1.142-1.084 (m, 7 H), 0.938-0.807 (m, 1 H), 0.791-0.766 (m, 6 H).

Aufarbeitung

  1. customPurification
  2. customto provide a solid (0.118 g, 124°-126° C.)

Quellen und Nachweise

ORD-Eintrag
ord-de089561c7f14dc78c3f8ea0b285337c
Quelldatensatz
uspto-grants-1998_11
Patentnummer
US05840751

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