반응 #670629

ord-39ac193396774e30aac0619e7060ac2c

반응 방정식

COc1ccc(Br)cc1OC
4-bromoveratrole
COc1ccc(C(=O)c2ccncc2)cc1OC
4-(3,4-dimethoxybenzoyl)pyridine
COc1cc(C#N)cc(OC)c1
3,5-dimethoxybenzonitrile
[Li][CH2]CCC
butyl lithium
COc1cc(OC)cc(C(=O)c2ccc(OC)c(OC)c2)c1
3,4,3',5'-Tetramethoxybenzophenone

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The crude product was purified by flash column chromatography (silica gel, methylene chloride)

실험 절차

3,4,3',5'-Tetramethoxybenzophenone was prepared analogously to 4-(3,4-dimethoxybenzoyl)pyridine using butyl lithium (9 mL, 22 mmol, 2.5M), 4-bromoveratrole (2.9 mL, 20 mmol) and 3,5-dimethoxybenzonitrile (3.75 g, 23 mmol). The crude product was purified by flash column chromatography (silica gel, methylene chloride) to afford 1.54 g (26%) of the product: mp 107-110° C.; 1H NMR (CDCl3) δ 7.53-7.39 (m, 2H), 6.95-6.84 (m, 3H), 6.70-6.60 (m, 1H), 3.96 (s, 3H), 3.95 (s, 3H), 3.83 (s, 6H); 13C NMR (CDCl3) δ 195.0, 160.4, 153.0, 148.9, 140.1, 130.0, 125.4, 112.0, 109.7, 107.5, 104.1, 56.0, 55.5; Anal. Calcd for C17H18O5. Theoretical: C, 67.54; H, 6.00. Found: C, 67.38; H, 5.96.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05929117uspto-grants-1999_07