Реакция #42224

ord-45402095ab7d402f83ad407b94806d78

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

Treatment of 5-allyl-6-chloroindan-4-ol (4.5 g, 0.0216 mol) with sodium hydride (60 wt. %, 1.32 g, 0.033 mol) followed by benzyl bromide (6.0 g, 0.035 mol) generally according to the procedure described for Intermediate 38 gave 5.76 g (89%) of 5-allyl-4-(benzyloxy)-6-chloroindane as a colorless oil. 1H NMR (CDCl3) 8H 7.40 (m, 5H); 7.05 (s, 1H); 6.00 (m, 1H); 5.00(m, 2H); 4.90 (s, 2H); 3.53 (dd, 2H); 2.90 (m, 4H); 2.05 (m, 2H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07728155B2uspto-grants-2010_06