Реакция #78304

ord-3dcc60becf714af6bbd5177c23888703

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

According to the procedure of Method A, Example 1, (E)-2-methyl-2-phenyl-5-[2-(3-thienyl)ethenyl]-3(2H)-furanone was reacted with 3-mercapto-1-propanol to provide 5-[2-[(3-hydroxypropyl)thio]-2-(3-thienyl)ethyl]-2-methyl-2-phenylfuran-3(2H)-one; 1H NMR (CDCl3) δ1.40 (br s, 1H), 1.65 and 1.68 (singlets, 3H), 1.68-1.82 (m, 2H), 2.42-2.57 (m, 2H), 3.10-3.27 (m, 2H), 3.67 (m, 2H), 4.42 (m, 1H), 5.37 and 5.39 (singlets, 1H), 7.05-7.18 (m, 2H), 7.27-7.40 (m, 6H); MS (HR-FAB) m/z 375.1113 (M+H calcd. for C20H23O3S2 375.1089).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06710078B2uspto-grants-2004_03