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

HRID 481916ノート

反応式

HRID 481916 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.[Cl:27][C:28]1[CH:36]=[CH:35][CH:34]=[CH:33][C:29]=1[C:30](Cl)=O.CC(C)(O)C#N.C([BH3-])#N.[Na+]>C(O)(=O)C.C(#N)C.C(Cl)Cl>[Cl:27][C:28]1[CH:36]=[CH:35][CH:34]=[CH:33][C:29]=1[CH2:30][C:3]1[C:4](=[O:19])[O:5][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)[CH2:7][C:2]=1[OH:1]

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-chlorobenzoyl chloride (0.15 mL, 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 (4.0 mL), sodium cyanoborohydride (0.720 g, 11.5 mmol). Purification was achieved by submitting the final residue to column chromatograpy (SiO2, 100% CH2Cl2) to provide a solid (0.165 g, 51°-53° C.). 1H NMR (400 MHz, DMSO-d6) δ11.062 (bs, 1H), 7.425-7.275 (m, 6H), 7.072 (td, 1H, J=1.5 Hz, J=7.5 Hz), 6.774 (td, 1H, J=1.2 Hz, J=7.5 Hz), 6.059 (dd, 1H, J=1.2 Hz, J=7.5 Hz), 3.428 (AB, 2H, JAB =16.5 Hz), 3.191 (AB, 2H, JAB=17 Hz), 1.964-1.884 (m, 2H), 1.450-1.384 (m, 1H), 1.163-1.118 (m, 1H), 0.951 (m, 1H), 0.802-0.776 (m, 6H).

後処理

  1. customPurification
  2. customto provide a solid (0.165 g, 51°-53° C.)

出典と根拠

ORDレコード
ord-1d7ab3c94c704199b63e636fa5f9124a
出典データセット
uspto-grants-1998_08
特許番号
US05789440

反応ノート

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