1-Naphthol → (2R)-1-(butyryloxy)-3-(1-naphthyloxy)-2-propanol
反応式
[C:1]1([OH:11])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[C:12]([O:17][CH2:18][C@@H:19]1[O:21][CH2:20]1)(=[O:16])[CH2:13][CH2:14][CH3:15]>[I-].C([N+](CCCC)(CCCC)CCCC)CCC.C1(C)C=CC=CC=1>[C:12]([O:17][CH2:18][C@H:19]([OH:21])[CH2:20][O:11][C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1)(=[O:16])[CH2:13][CH2:14][CH3:15]参加物
5
実験手順
To a solution of 144 g (1 mol) of 1-naphthol and 7.4 g (0.02 mol) of tetrabutylammonium iodide in 200 ml of toluene was added 144 g (1 mol) of (R)-glycidyl butyrate over a period of 15 min at a temperature of 120° C., and the mixture was kept at this temperature for a further 4 h. Conventional subsequent treatment of the reaction mixture gave the required compound as an oil, yield about 75%.