反应详情

222 Parts of redistilled tetrahydrofuran is cooled to 0° and then treated with 15.6 parts by volume of 1M lithium aluminum hydride in tetrahydrofuran. The temperature of that mixture is lowered to -70° and 6.92 parts of methyl 2-methoxy-4-hydroxy-5-oxocyclopent-1-eneheptanoate dissolved in 53 parts of tetrahydrofuran is added. The addition takes place over a 2 minute period and the temperature of the reaction mixture is not allowed to rise above -60°. After the addition is complete, the temperature is lowered to -70° and the reaction mixture is stirred for 41/2 hours. Then 4 parts of methanol and 8.9 parts of tetrahydrofuran is added and the temperature of the reaction mixture is allowed to rise to -20° at which time 60 parts by volume of a 1 N hydrochloric acid solution is slowly added. The resulting mixture is allowed to stand for 16 hours at a temperature of about 4°. Then the solvent is removed under reduced pressure and the residue which remains is diluted with ethyl acetate. The aqueous and organic layers which form are separated and the organic layer is washed with water, potassium bicarbonate and water and dried over anhydrous sodium sulfate. After the solvent is removed under reduced pressure, the remaining material is chromatographed on silicic acid with ethyl acetate-benzene (1:4) as eluant to afford methyl 3-hydroxy-5-oxocylopent-1-eneheptanoate.

1. customis lowered to -70°
2. additionis added
3. additionThe addition
4. customover a 2 minute
5. customto rise above -60°
6. additionAfter the addition
7. customis lowered to -70°
8. additionis slowly added
9. waitto stand for 16 hours at a temperature of about 4°
10. customThen the solvent is removed under reduced pressure
11. additionthe residue which remains is diluted with ethyl acetate
12. customThe aqueous and organic layers which form are separated
13. washthe organic layer is washed with water, potassium bicarbonate and water
14. dry with materialdried over anhydrous sodium sulfate
15. customAfter the solvent is removed under reduced pressure
16. customthe remaining material is chromatographed on silicic acid with ethyl acetate-benzene (1:4) as eluant