Triisopropyl borate → 5-Allyl-2-hydroxy-3-methoxyphenylboronic acid
反応式
[CH2:1]([C:4]1[CH:16]=[CH:15][C:7]([O:8]C2CCCCO2)=[C:6]([O:17][CH3:18])[CH:5]=1)[CH:2]=[CH2:3].C([Li])(CC)C.C([O:27][B:28](OC(C)C)[O:29]C(C)C)(C)C>C1COCC1>[CH2:1]([C:4]1[CH:5]=[C:6]([O:17][CH3:18])[C:7]([OH:8])=[C:15]([B:28]([OH:29])[OH:27])[CH:16]=1)[CH:2]=[CH2:3]参加物
5
実験手順
2-(4-Allyl-2-methoxyphenoxy)tetrahydropyran (2.0 g, 8.05 mmol) was dissolved in dry THF (70 ml) and the solution cooled to −78° C. sec-Butyl lithium (1.3M in hexanes, 7.4 ml, 9.62 mmol) was added dropwise with stirring over 10 minutes, the reaction was stirred at −78° C. for 2 hours. Triisopropoxy borane (3.4 ml, 14.6 mmol) was added and stirring continued for 4hours at −78° C. The reaction was quenched with water, acidified to pH 1 with 2N hydrochloric acid and extracted with ether (2×200 ml). The combined extracts were dried with magnesium sulphate and concentrated under vacuum. The oily solid produced was triturated with cyclohexane and the solid filtered off to give the title compound (41%); MS 207 (M-H)−; HPLC retention time (system 1) 2.73 minutes.