反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
At -78° C., to a stirred solution of (2-ethyl-benzofuran-3-yl)-(2'-methoxy-[1,1';3',1"]terphenyl-5'-yl)-methanone (1.07 g, 2.47 mmol) in CH2Cl2 (10.1 mL) was added dropwise 1M boron tribromide/CH2Cl2 (5.2 mL). After the addition was complete, the dry ice/acetone bath was replaced with an ice water bath and the reaction was stirred for 72 h, eventually warming to ambient temperature. The reaction was carefully quenched with crushed ice, diluted with H2O (16 mL) and extracted with ether. The ethereal extracts were dried (MgSO4) and concentrated. Purification on Biotage KP-Sil eluting with 15% acetone/hexane gave 0.86 g, (83%) of the title compound as a white solid, mp 142-143° C. 1H NMR (DMSO-d6) δ 1.24 (t, 3 H), 2.90 (quartet, 2 H), 7.28-7.66 (m, 16 H), 9.37 (s, 1 H). IR (KBr) 3200, 2950, 1625, 1560 and 1175 cm-1. mass spectrum (EI), m/z 418 (M+). Anal. Calcd. for C29H22O3.0.35H2O: C, 82.00; H, 5.39; N, 0.00. Found: C, 82.06; H, 5.40; N, 0.07.
WORKUP
后处理
- additionAfter the addition
- customThe reaction was carefully quenched with crushed ice
- additiondiluted with H2O (16 mL)
- extractionextracted with ether
- dry with materialThe ethereal extracts were dried (MgSO4)
- concentrationconcentrated
- customPurification on Biotage KP-Sil
- washeluting with 15% acetone/hexane