反応式
[CH3:1][O:2][C:3](=[O:27])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C@@H:10]1[C@@H:14](/[CH:15]=[CH:16]/[CH2:17][C:18]([OH:24])([CH3:23])[CH2:19][CH2:20][CH2:21][CH3:22])[C@H:13]([OH:25])[CH2:12][C:11]1=[O:26]>C(O)C.[Pd]>[CH3:1][O:2][C:3](=[O:27])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C@@H:10]1[C@@H:14]([CH2:15][CH2:16][CH2:17][C:18]([OH:24])([CH3:23])[CH2:19][CH2:20][CH2:21][CH3:22])[C@H:13]([OH:25])[CH2:12][C:11]1=[O:26]参加物
4
実験手順
(±) methyl-11α,16-dihydroxy-16-methyl-9-oxoprost-13E-en-1-oate (100 mg) in 15 ml of ethanol containing 100 mg of 4% palladium on carbon is hydrogenated at room temperature and atmospheric pressure for 24 minutes. The solution is filtered and evaporated. The residue is chromatographed on silica gel (60% ethyl acetate/40% hexane as eluent) to give 86 mg of desired product as a viscous oil. 1H NMR (CDCl3): ∂0.93 (t, C.20 CH3); 1.18 (d, C.16 CH3 ; 3.68 (s, OCH3); 4.17 (q C.11 H).
後処理
- customis hydrogenated at room temperature
- filtrationThe solution is filtered
- customevaporated
- customThe residue is chromatographed on silica gel (60% ethyl acetate/40% hexane as eluent)
出典と根拠
- ORDレコード
- ord-6d668bc3bd22471b9b661f70c8a663dd
- 出典データセット
- uspto-grants-1992_10
- 特許番号
- US05157052
関連ノート
読み込み中…