反应 #89616

反应方程式

vitride

2,6-dimethyl-2-(2-methyl-allyl)-cyclohexanone

→

2,2,3a,7-tetramethyl-octahydro-benzofuran

收率 62.3%

溶剂

toluene

反应条件

后处理

1. 1
   其他A 3 L reaction flask
2. 2
   温度the reaction mixture was cooled to room temperature
3. 3
   其他quenched with IPA (100 mL)
4. 4
   workup.ADDITIONNaOH (50%, 300 g) and water (200 mL) were then added
5. 5
   温度heated to 80° C.
6. 6
   workup.WAITaged for another hour
7. 7
   温度The reaction mixture was cooled to room temperature
8. 8
   workup.ADDITIONmore water (200 mL) was added
9. 9
   其他Layers were split
10. 10
    workup.ADDITIONThe organic layer was charged back to the flask
11. 11
    workup.ADDITIONToluene (300 mL) was added
12. 12
    其他water was removed with a Bidwell-Sterling trap through azeotrope
13. 13
    温度The resulting mixture was cooled to 50° C
14. 14
    workup.ADDITIONMSA (28 g, 0.3 mol) was added
15. 15
    温度the reaction mixture was heated to reflux
16. 16
    其他The consumption of the starting material
17. 17
    workup.WAITwas indicated after 3 hours
18. 18
    温度The resulting mixture was then cooled to room temperature
19. 19
    洗涤washed with saturated sodium carbonate solution (1 L)
20. 20
    workup.DISTILLATIONDistillation and fractionation

实验过程

A 3 L reaction flask was charged with vitride (325 g, 0.9 mol) and toluene (500 mL), heated to 100° C., fed with 2,6-dimethyl-2-(2-methyl-allyl)-cyclohexanone (200 g, 1.1 mol, obtained as detailed above) for over 2 hours, and aged for another 2 hours. After the reaction completed, the reaction mixture was cooled to room temperature, quenched with IPA (100 mL). NaOH (50%, 300 g) and water (200 mL) were then added, heated to 80° C., and aged for another hour. The reaction mixture was cooled to room temperature and more water (200 mL) was added. Layers were split to dispose the aqueous waste. The organic layer was charged back to the flask. Toluene (300 mL) was added and water was removed with a Bidwell-Sterling trap through azeotrope. The resulting mixture was cooled to 50° C. MSA (28 g, 0.3 mol) was added and the reaction mixture was heated to reflux. The consumption of the starting material was indicated after 3 hours. The resulting mixture was then cooled to room temperature and washed with saturated sodium carbonate solution (1 L) followed by brine (1 L). Distillation and fractionation provided the product 2,2,3a,7-tetramethyl-octahydro-benzofuran (125 g).

来源