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

HRID 357887ノート

反応式

HRID 357887 の反応式
[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]

参加物

9

実験手順

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).

後処理

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

出典と根拠

ORDレコード
ord-de089561c7f14dc78c3f8ea0b285337c
出典データセット
uspto-grants-1998_11
特許番号
US05840751

反応ノート

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