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 (1R, 2S, 4R)-2-Hydroxy-4-methyl-cyclohexanecarboxylic acid (162 mg, 1.02 mmol) in dichloromethane (5 ml) was added pyridine (495 ul, 6.12 mmol) followed by acetic anhydride (385 ul, 4.08 mmol). The reaction mixture was stirred for 20 h at room temperature. Then, the solvents were removed and 10 ml of 3N HCl solution was added. This mixture was stirred for 30 minutes and then a saturated solution of NaHCO3 was slowly added until PH=9-10. This solution was then extracted with ethyl acetate (2×5 ml). The aqueous phase was then acidified with a 10% HCl solution and extracted with ethyl acetate (3×5 ml). The following ethyl acetate layers were combined, dried (Na2SO4) and concentrated to obtain 109 mg (53%) of (1R, 2S, 4R)-2-Acetoxy-4-methyl-cyclohexanecarboxylic acid.
WORKUP
后处理
- customThen, the solvents were removed
- addition10 ml of 3N HCl solution was added
- stirringThis mixture was stirred for 30 minutes
- additiona saturated solution of NaHCO3 was slowly added until PH=9-10
- extractionThis solution was then extracted with ethyl acetate (2×5 ml)
- extractionextracted with ethyl acetate (3×5 ml)
- dry with materialdried (Na2SO4)
- concentrationconcentrated