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
Absolute ethanol was degassed by applying a vacuum while simultaneously bubbling nitrogen through it. A solution of 188 mg (0.5201 mmol) ethyl 6-[2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronapth-2-yl)ethynyl]-nicotinoate in 2 ml absolute ethanol was treated with 800 ml of a 1.65M (1.32 mmol) solution of potassium hydroxide in ethanol and water. The mixture was stirred at room temperature for 18 hours and then the solvent removed in vacuo. The residue was dissolved in water and extracted with 50 ml ether, which was discarded. The aqueous layer was then acidified with glacial acetic acid and extracted with 4×50 ml ether. The ether extracts were combined, washed with water, saturated NaCl solution and then dried (MgSO4). Solvent was removed in vacuo to give the title compound as a pale yellow solid. PMR (CDCl3): δ1.31 (12 H, s), 1.71(4 H, s), 7.34 (1 H, d, J~7.8 Hz), 7.40 (1 H, d, J~7.8 Hz), 7.62 (1 H, s), 8.39 (1 H, dd, J~7.3 Hz, 2.1 Hz), 9.33 (1 H, d, J~2.1 Hz).
WORKUP
后处理
- customAbsolute ethanol was degassed
- customthe solvent removed in vacuo
- dissolutionThe residue was dissolved in water
- extractionextracted with 50 ml ether, which
- extractionextracted with 4×50 ml ether
- washwashed with water, saturated NaCl solution
- dry with materialdried (MgSO4)
- customSolvent was removed in vacuo