HRID417694
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
(6′-Hydroxymethyl-4,6,2′,4% tetramethoxy-biphenyl-2-yl)-methanol: 4,6,4′,6′-tetramethoxy-biphenyl-2,2′-dicarboxylic acid dimethyl ester (2.5 g) was dissolved in THF (96 mL), and 1M LiAlH4 in THF (9.6 mL) was added. After stirring at room temperature for overnight, the mixture was quenched with water and 2N HCl (24 mL) was added. The mixture was evaporated under vacuum and partitioned with DCM (300 mL) and water (200 mL). The organic layer was dried over Na2SO4 and crystallized with DCM to provide (6′-hydroxymethyl-4,6,2′,4′-tetramethoxy-biphenyl-2-yl)-methanol (1.7 g, 77%) as a pale blue white triclinic crystals.
WORKUP
后处理
- customthe mixture was quenched with water and 2N HCl (24 mL)
- additionwas added
- customThe mixture was evaporated under vacuum
- custompartitioned with DCM (300 mL) and water (200 mL)
- dry with materialThe organic layer was dried over Na2SO4
- customcrystallized with DCM