反応 #6083

反応方程式

ethyl 6-[2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronapth-2-yl)ethynyl]-nicotinoate

potassium hydroxide

→

title compound

6-[2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphth-2-yl)ethynyl]nicotinic acid

溶媒

ethanol

ethanol

water

反応条件

後処理

1. 1
   その他Absolute ethanol was degassed
2. 2
   その他the solvent removed in vacuo
3. 3
   workup.DISSOLUTIONThe residue was dissolved in water
4. 4
   抽出extracted with 50 ml ether, which
5. 5
   抽出extracted with 4×50 ml ether
6. 6
   洗浄washed with water, saturated NaCl solution
7. 7
   乾燥dried (MgSO4)
8. 8
   その他Solvent was removed in vacuo

実験手順

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).

出典