반응 #89616

반응 방정식

vitride

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

→

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

수율 62.3%

용매

toluene

반응 조건

후처리

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

실험 절차

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).

출처