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
2,6-Bis-dimethoxyphenyllithium was prepared from 14.18 g (0.103 mole) of 1,3-dimethoxybenzene, 77 mL of a 1.6 M solution of BuLi in hexanes and 0.23 mL of N,N,N′,N′-tetramethylethylenediamine in dry diethyl ether (72 mL). Dichloromethylphosphine (5.0 g, 0.04276 mole) was added at 0° C., and the reaction mixture was stirred at room temperature overnight. Methanol (20 mL) was added, and the mixture was concentrated to about half its original volume under reduced pressure. The resulting white precipitates were filtered and were recrystallized from methanol to give white crystals of bis-(2,6-dimethoxyphenyl)(methyl)-phosphine with 48% yield (6.6 g) and melting point at 112.33° C. 1H NMR (CDCl3) δ 1.75 (s(broad), 3H, Me-P), 3.55 (s, 12H, Me-O), 6.4-7.2 (m, 6H, aromatic protons); 31P NMR (CDCl3)δ-51.5 ppm. LS/MS: found m/w is 321, calculated m/w is 321. Anal. found: C 64.30%; H 6.45%; calculated for C17H22O4P: C 63.49%; H 6.85%.
WORKUP
后处理
- concentrationthe mixture was concentrated to about half its original volume under reduced pressure
- customThe resulting white precipitates
- filtrationwere filtered
- customwere recrystallized from methanol