Toluene → (R)-4-methyl-4-(6-(4-pentylcyclohexyloxy)naphthalen-2-yl)oxazolidin-2-one
反応式
[CH2:1]([CH:6]1[CH2:11][CH2:10][CH:9]([OH:12])[CH2:8][CH2:7]1)[CH2:2][CH2:3][CH2:4][CH3:5].O1CCCC1.O[C:19]1[CH:20]=[C:21]2[C:26](=[CH:27][CH:28]=1)[CH:25]=[C:24]([C@:29]1([CH3:35])[CH2:33][O:32][C:31](=[O:34])[NH:30]1)[CH:23]=[CH:22]2.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OCC)=O)=NC(OCC)=O.C1(C)C=CC=CC=1.CCOC(/N=N/C(OCC)=O)=O>>[CH3:35][C@@:29]1([C:24]2[CH:23]=[CH:22][C:21]3[C:26](=[CH:27][CH:28]=[C:19]([O:12][CH:9]4[CH2:8][CH2:7][CH:6]([CH2:1][CH2:2][CH2:3][CH2:4][CH3:5])[CH2:11][CH2:10]4)[CH:20]=3)[CH:25]=2)[CH2:33][O:32][C:31](=[O:34])[NH:30]1参加物
8
反応物 7
生成物 1
実験手順
In a 40 mL vial, 4-Pentyl-cyclohexanol (1144.4 mg, 0.0067202 mol) was diluted with tetrahydrofuran (30.0 mL, 0.370 mol, Acros) and subsequently (R)-4-(6-hydroxynaphthalen-2-yl)-4-methyloxazolidin-2-one (1.4924 g, 0.0061350 mol) and triphenylphosphine (2105.5 mg, 0.0080275 mol) were added and the mixture was stirred. Diethyl Azodicarboxylate in toluene (2.6 mL, 0.0086326 mol, Aldrich) was added, and the mixture was then stirred at room temperature for 38 h. The reaction mixture was evaporated to dryness and chromatographed 0-100% EtOAc/Hexanes (adsorbed onto silica gel). Isolated was 0.6142 g (18%) in approx 70% purity, the remainder being reduced DEAD reagent.
後処理
- additionwere added
- stirringthe mixture was then stirred at room temperature for 38 h
- customThe reaction mixture was evaporated to dryness
- customchromatographed 0-100% EtOAc/Hexanes (adsorbed onto silica gel)
- customIsolated
出典と根拠
- ORDレコード
- ord-50a3bf3819c54405854819d6f6526ab2
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08546359B2
反応ノート
読み込み中…