Trifluoroacetic acid → 2-{3-Methoxy-2-propoxy-5-[5-(3,4,5-trimethoxyphenyl)oxolan-2-yl]benzene-1-sulfonyl}ethan-1-ol

反応式

F[C:2](F)(F)[C:3]([OH:5])=O.[OH:8][CH2:9][CH2:10][S:11]([C:14]1[C:15](OCCC)=[C:16]([O:38][CH3:39])[CH:17]=[C:18]([CH:20](O)[CH2:21][CH2:22][CH:23]([C:25]2[CH:30]=[C:29]([O:31][CH3:32])[C:28]([O:33][CH3:34])=[C:27]([O:35][CH3:36])[CH:26]=2)[OH:24])[CH:19]=1)(=[O:13])=[O:12].[C:44]([O-])([O-])=O.[Na+].[Na+]>C(Cl)(Cl)Cl>[OH:8][CH2:9][CH2:10][S:11]([C:14]1[C:15]([O:5][CH2:3][CH2:2][CH3:44])=[C:16]([O:38][CH3:39])[CH:17]=[C:18]([C@H:20]2[CH2:21][CH2:22][C@H:23]([C:25]3[CH:30]=[C:29]([O:31][CH3:32])[C:28]([O:33][CH3:34])=[C:27]([O:35][CH3:36])[CH:26]=3)[O:24]2)[CH:19]=1)(=[O:13])=[O:12]

参加物

実験手順

Trifluoroacetic acid (10%, v/v) in chloroform (500 mL) was added to a stirred 0° C. solution of 1-(5-(2-hydroxyethylsulfonyl)-4-n-propoxy-3-methoxyphenyl)-4-(3,4,5-trimethoxyphenyl) butan-1,4-diol (75 g, 0.142 mole) in chloroform (500 mL). The temperature was slowly raised to room temperature and the mixture stirred for 3-4 hours. Anhydrous Na2CO3 (80 g, 0.75 mole) was added to this solution, and the mixture was stirred vigorously for 30 minutes. The solid was filtered off, and the filtrate was evaporated to a residue, which was purified by flash column chromatography on SiO2 eluted with hexane-ethyl acetate (6:1, v/v) to afford the desired trans isomer which is more mobile than the cis isomer. The product was recrystallized from methylene chloride-hexane to give of pure trans-2-(5-(2-hydroxyethylsulphonyl)-4-n-propoxy-3-methoxyphenyl)-5-(3,4,5-trimethoxyphenyl)tetrahydrofuran, m.p. 141°-142° C. NMR (CDCl3) δ: 1.03 (t, J=7.8 Hz, CH2CH2CH3), 1.85 (m, CH2CH2CH3), 2.01, 2.46 (m, H-3 and H-4), 3.64 (m, SO2CH2CH2OH) 3.84, 3.86, 3.88 (35, 4 OCH3), 4.89 (m, SO2CH2CH2OH), 4.07 (t, J=8 Hz, OCH2CH2CH3), 5.13 (m, H-2 and H-5) 6.62 (s, Ar-H H-2 and H-6), 7.32 (d, J=2 Hz, Ar-H H-6), 7.52 (d, J=2 Hz, Ar-H H-2).