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
CONDITIONS
反应条件
- 温度
- -90 °C
PROCEDURE
实验过程
A solution of butyllithium (18.17 ml, 2.5M in hexanes) was added to 4-bromo-1-tetrahydropyran-2-yl-pyrazole, in solution in THF (400 ml) between −100° C. and −80° C. under nitrogen atmosphere. The mixture was stirred for 1 hour at −90° C. Trimethoxyborane (5.07 ml) was added at −70° C. and the mixture was stirred for a further 30 minutes. The mixture was quenched with a 15% solution of ammonium chloride (5 ml); the mixture was allowed to warm to room temperature and was stirred for 30 minutes. The organic layer was separated and the aqueous layer was extracted with 20 ml of THF. The combined organic portions were dried over magnesium sulphate and the solvent was evaporated under reduce pressure to afford the crude boronic acid. 2,3-dimethylbutane-2,3-diol (5.11 g) was added to the boronic acid in solution in THF with 4 A molecular sieves (100 mg). The mixture was stirred at room temperature for 15 hours. The mixture was evaporated under reduce pressure. Water (5 ml) was added and the mixture was extracted with heptane (3×10 ml), dried over magnesium sulphate, filtered and evaporated under reduce pressure to afford 1-tetrahydropyran-2-yl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole (8.80 g). NMR Spectrum: (CDCl3) 1.31 (s, 1H), 1.54-1.76 (m, 4H), 1.95-2.17 (m, 2H), 3.66-3.73 (m, 1H), 4.01-4.07 (m, 1H), 5.41 (dd, 1H), 7.82 (s, 1H), 7.94 (s, 1H)
WORKUP
后处理
- stirringthe mixture was stirred for a further 30 minutes
- customThe mixture was quenched with a 15% solution of ammonium chloride (5 ml)
- temperatureto warm to room temperature
- stirringwas stirred for 30 minutes
- customThe organic layer was separated
- extractionthe aqueous layer was extracted with 20 ml of THF
- dry with materialThe combined organic portions were dried over magnesium sulphate
- customthe solvent was evaporated
- customto afford the crude boronic acid
- stirringThe mixture was stirred at room temperature for 15 hours
- customThe mixture was evaporated
- additionWater (5 ml) was added
- extractionthe mixture was extracted with heptane (3×10 ml)
- dry with materialdried over magnesium sulphate
- filtrationfiltered
- customevaporated