反応 #65056

反応方程式

benzaldehyde

sodium hydroxide

3-acetyl-5-butyldihydro-2(3H)-furanone

water

→

(E)-3-(phenylmethylene)-5-butyldihydro-2 (3H)-furanone

収率 64.5%

溶媒

toluene

反応条件

後処理

1. 1
   workup.ADDITIONcharged to a 500 mL flask
2. 2
   その他fitted with a mechanical stirrer
3. 3
   その他was removed in the Dean-Stark trap
4. 4
   温度The reaction was further heated
5. 5
   温度under reflux for an additional 2.5 hours
6. 6
   温度The reaction mixture was then cooled to room temperature
7. 7
   洗浄washed with 3×80 ml of water
8. 8
   抽出The water layer was extracted with 50 ml of toluene
9. 9
   洗浄The toluene solution was then washed with 100 ml of saturated sodium chloride
10. 10
    乾燥dried over Na2SO4
11. 11
    濃縮concentrated to 35.4 gms of an orange oil under rotoevaporation
12. 12
    workup.DISTILLATION19.0 gms of this oil was subjected to simple straight takeover distillation (0.04 mm Hg: 25°-147° C.)

実験手順

To a mixture of 36.8 g (0.200 mole) of 3-acetyl-5-butyldihydro-2(3H)-furanone in 200 mL of toluene charged to a 500 mL flask fitted with a mechanical stirrer, Dean-Stark trap and an addition funnel was added 8.00 g (0.200 mole) of sodium hydroxide at once. The mixture was vigorously stirred for 10 mins. at room temperature and then heated under reflux for 1 hour while water was removed in the Dean-Stark trap. After the one hour period 23.9 g (0.225 mole) of benzaldehyde was added to the refluxing solution in 4-5 ml aliquats in 1 hour. The reaction was further heated under reflux for an additional 2.5 hours. The reaction mixture was then cooled to room temperature and washed with 3×80 ml of water. The water layer was extracted with 50 ml of toluene and the toluene layers combined. The toluene solution was then washed with 100 ml of saturated sodium chloride and dried over Na2SO4 and concentrated to 35.4 gms of an orange oil under rotoevaporation. 19.0 gms of this oil was subjected to simple straight takeover distillation (0.04 mm Hg: 25°-147° C.) to leave 16 g (64.5% yield) of (E)-3-(phenylmethylene)-5-butyldihydro-2 (3H)-furanone as a viscous liquid. 1HNMR (CDCl3) δ7.5 (m, 6H), 4.56 (pentet, 1H), 3.3 (ddd, 1H), 2.8 (ddd, 1H), 1.9-1.2 (m, 6H), 0.86 (t, 3H).

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