반응 #164005

ord-8b865e356b1a46beaac9524639b9f9ac

반응 방정식

COc1cc(O)cc(OC)c1
3,5-dimethoxyphenol
COc1cc(C(=O)CBr)cc(OC)c1OC
2-bromo-1-(3,4,5-trimethoxyphenyl)ethanone
COc1cc(OC)c2cc(-c3cc(OC)c(OC)c(OC)c3)oc2c1
4,6-dimethoxy-2-(3,4,5-trimethoxyphenyl)-1-benzofuran
수율 75.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타This compound was prepared

실험 절차

This compound was prepared using Method A from 3,5-dimethoxyphenol and 2-bromo-1-(3,4,5-trimethoxyphenyl)ethanone: Yield 75% following procedure A.2; m.p. 131-132° C.; IR 2960, 1619, 1497, 1227, 1203, 1134, 1110 cm−1; 1H-NMR (500 MHz, δ ppm, CDCl3) 7.04 (s, 2H), 7.00 (s, 1H), 6.74 (s, 1H), 6.36 (d, J=1.8 Hz, 1H), 3.97 (s, 6H), 3.95 (s, 3H), 3.91 (s, 3H), 3.89 (s, 3H); 13C-NMR (126 MHz, δ ppm, CDCl3) 159.4, 156.7, 153.8, 153.7, 153.6, 138.4, 126.6, 113.5, 101.9, 98.7, 94.6, 88.5, 61.2, 56.4, 56.0, 55.8.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08835659B2uspto-grants-2014_09