HRID11931
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 solution of 0.23 g (0.49 mmol) (4R,9aR)-6-(benzhydrylidene-amino)-4-methyl-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester in 2.5 ml methanol were added 0.46 g (7.4 mmol) ammonium formate and 104 mg (0.05 mmol) 5% palladium on charcoal and the suspension was stirred for 1 h at 60 deg C. The cooled reaction mixture was filtered through a short bed of dicalite speed plus, extracted with 10% aqueous sodium bicarbonate, brine, dried over magnesium sulfate, filtered and evaporated. The residue was purified by chromatography on silica gel (0.032–0.063 mm) to yield the product as a colorless oil (58.9%).
WORKUP
后处理
- customThe cooled reaction mixture
- filtrationwas filtered through a short bed of dicalite speed
- extractionextracted with 10% aqueous sodium bicarbonate, brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- customevaporated
- customThe residue was purified by chromatography on silica gel (0.032–0.063 mm)