Реакция #42216

ord-b8e797c240de4e019d869b0001db58ea

Уравнение реакции

COc1cc(CC(O)COS(=O)(=O)c2ccc(C)cc2)c(O)c2c1C1CCC2CC1
(±)-2-hydroxy-3-(5-hydroxy-8-methoxy-1,2,3,4-tetrahydro-1,4-ethanonaphthalen-6-yl)propyl 4-methylbenzenesulfonate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CCOC(=O)/N=N/C(=O)OCC
diethylazodicarboxylate
COc1cc2c(c3c1C1CCC3CC1)OC(COS(=O)(=O)c1ccc(C)cc1)C2
(±)-(5-methoxy-2,3,6,7,8,9-hexahydro-6,9-ethanonaphtho[1,2-b]furan-2-yl)methyl 4-methylbenzenesulfonate
Выход 75.1%

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

Treatment of (±)-2-hydroxy-3-(5-hydroxy-8-methoxy-1,2,3,4-tetrahydro-1,4-ethanonaphthalen-6-yl)propyl 4-methylbenzenesulfonate (15.14 g, 35.0 mmol) with triphenylphosphine (10.10 g, 38.5 mmol) followed by diethylazodicarboxylate (6.71 g, 38.5 mmol) generally according to the procedure described for Intermediate 5 afforded 10.9 g (75%) of (±)-(5-methoxy-2,3,6,7,8,9-hexahydro-6,9-ethanonaphtho[1,2-b]furan-2-yl)methyl 4-methylbenzenesulfonate as a white solid. mp 136-141° C.; Anal. calcd. for C23H26O5S: C, 66.64; H, 6.32. Found: C, 66.53; H, 6.51.

Источник

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