反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a stirred suspension of zinc powder (23.4 g, 0.36 mol) in THF (300 mL) was slowly added TiCl4 (20 mL, 0.18 mol) via a syringe at room temperature under a nitrogen atmosphere. The reaction mixture was heated at reflux for 1 h. A solution of (4-bromophenyl)(4-hydroxyphenyl)methanone (2) (10.0 g, 0.036 mol) and 3,3,5,5-tetramethylcyclohexanone (16.7 g, 0.108 mol) in THF (100 mL) was added to the reaction mixture. The reaction mixture was heated at reflux with stirring under a nitrogen atmosphere for an additional 2 h. The reaction mixture was allowed to cool to room temperature. To the reaction mixture was poured into a 10% aqueous K2CO3 (1 L). The reaction mixture was filtered through a pad of Celite and the pad was washed with EtOAc. The filtrate was transferred to a separatory funnel and the layers were separated. The aqueous phase was further extracted with EtOAc (4×250 mL). The combined organic phase was washed with brine (2×100 mL), dried (Na2SO4), filtered, and then filtrate was concentrated under reduced pressure to give the crude product as a gold-yellow oil. The crude product was purified by flash chromatography on silica gel with hexanes:EtOAc (100:0 to 1:1) as an eluent to afford 10.45 g (73%) of compound 14 as a white solid. 1H NMR (300 MHz, CDCl3): δ 0.91 (s, 6H), 0.95 (s, 6H), 1.31 (s, 2H), 1.96 (s, 2H), 1.99 (s, 2H), 4.67 (s, 1H), 6.76 (d, J=8.7 Hz, 2H), 7.03 (d, J=6.0 Hz, 2H), 7.05 (d, J=6.0 Hz, 2H), 7.41(d, J=8.4 Hz, 2H). HRMS (EI) Calcd for C23H27BrO: 398.1245 (M+.). Found: 398.1248.
WORKUP
后处理
- customat room temperature
- temperatureThe reaction mixture was heated
- temperatureat reflux for 1 h
- temperatureThe reaction mixture was heated
- temperatureat reflux
- filtrationThe reaction mixture was filtered through a pad of Celite
- washthe pad was washed with EtOAc
- customThe filtrate was transferred to a separatory funnel
- customthe layers were separated
- extractionThe aqueous phase was further extracted with EtOAc (4×250 mL)
- washThe combined organic phase was washed with brine (2×100 mL)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationfiltrate was concentrated under reduced pressure