Technology Process of 2aβ,4aβ,5,6,7,8,8aβ,8bβ-octahydro-2-benzyl-2H,3H-thieno<3',4',5':3,3a,4>cycloheptisoxazole
There total 5 articles about 2aβ,4aβ,5,6,7,8,8aβ,8bβ-octahydro-2-benzyl-2H,3H-thieno<3',4',5':3,3a,4>cycloheptisoxazole which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
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66202-12-8
2aβ,4aβ,5,6,7,8,8aβ,8bβ-octahydro-2-benzyl-2H,3H-thieno<3',4',5':3,3a,4>cycloheptisoxazole
- Guidance literature:
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With
triethylamine;
In
acetonitrile;
for 2h;
Heating;
DOI:10.1021/ja00526a033
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-
66202-12-8
2aβ,4aβ,5,6,7,8,8aβ,8bβ-octahydro-2-benzyl-2H,3H-thieno<3',4',5':3,3a,4>cycloheptisoxazole
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 71 percent / triethylamine / acetonitrile / 2 h / 25 °C / edducts were added at 0 deg C
2: 1.) sodium ethoxide / 1.) ethanol, reflux, 0.25 h, 2.) 2 h
3: 100 percent / p-toluenesulfonic acid hydrate / acetone; H2O / 1 h / Heating
4: 66 percent / triethylamine / acetonitrile / 2 h / Heating
With
sodium ethanolate; toluene-4-sulfonic acid; triethylamine;
In
water; acetone; acetonitrile;
DOI:10.1021/ja00526a033
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-
66202-12-8
2aβ,4aβ,5,6,7,8,8aβ,8bβ-octahydro-2-benzyl-2H,3H-thieno<3',4',5':3,3a,4>cycloheptisoxazole
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 1.) sodium ethoxide / 1.) ethanol, reflux, 0.25 h, 2.) 2 h
2: 100 percent / p-toluenesulfonic acid hydrate / acetone; H2O / 1 h / Heating
3: 66 percent / triethylamine / acetonitrile / 2 h / Heating
With
sodium ethanolate; toluene-4-sulfonic acid; triethylamine;
In
water; acetone; acetonitrile;
DOI:10.1021/ja00526a033
