Technology Process of 14,17-Cycloethano-norcodeinondimethylacetal-benzyl-hydroxyd
There total 9 articles about 14,17-Cycloethano-norcodeinondimethylacetal-benzyl-hydroxyd which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 8 steps
1: 92 percent / K2CO3 / acetone / 0.5 h / Heating
2: 83 percent / bromacetamide / CH2Cl2
3: 61 percent / 4 N NaOH, H2 / Pd/C (10 percent Pd) / methanol / 3.5 h
4: 64 percent / xylene / 12 h / Heating
5: 1) 1 M LiAlH4, 2) NaBH4 / 1) THF, reflux, 2 h, 2) methanol
6: 84 percent / methanol / 0.17 h
7: 93 percent / methanol / 3 h / Heating
8: 72 percent / Ag2O, H2O / 0.5 h
With
sodium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; bromo-acetic acid amide; water; hydrogen; potassium carbonate; silver(l) oxide;
10% palladium on active carbon;
In
methanol; dichloromethane; acetone; xylene;
DOI:10.1007/BF00812333
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 61 percent / 4 N NaOH, H2 / Pd/C (10 percent Pd) / methanol / 3.5 h
2: 64 percent / xylene / 12 h / Heating
3: 1) 1 M LiAlH4, 2) NaBH4 / 1) THF, reflux, 2 h, 2) methanol
4: 84 percent / methanol / 0.17 h
5: 93 percent / methanol / 3 h / Heating
6: 72 percent / Ag2O, H2O / 0.5 h
With
sodium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; water; hydrogen; silver(l) oxide;
10% palladium on active carbon;
In
methanol; xylene;
DOI:10.1007/BF00812333