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C21H30O3

Base Information Edit
C<sub>21</sub>H<sub>30</sub>O<sub>3</sub>

Synonyms:C21H30O3

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C21H30O3 Edit
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Technology Process of C21H30O3

There total 11 articles about C21H30O3 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:
Guidance literature:
With pyridine; pyridine hydrogenfluoride; In tetrahydrofuran; at 40 ℃; for 3h;
DOI:10.1016/j.tetlet.2011.10.151
Guidance literature:
Multi-step reaction with 6 steps
1.1: Dess-Martin periodane / dichloromethane / 1 h / 0 °C
2.1: borane-THF; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole / tetrahydrofuran / 6 h / -40 °C
3.1: sodium bis(2-methoxyethoxy)aluminium dihydride / 4 h / 40 °C
3.2: 12 h / -78 - 0 °C
4.1: 2,6-dimethylpyridine / dichloromethane / 0.17 h / 20 °C
5.1: palladium diacetate; triethylamine; tris-(o-tolyl)phosphine / water; acetonitrile / 1.5 h / 80 °C
6.1: pyridine; pyridine hydrogenfluoride / tetrahydrofuran / 3 h / 40 °C
With pyridine; 2,6-dimethylpyridine; borane-THF; palladium diacetate; Dess-Martin periodane; pyridine hydrogenfluoride; triethylamine; sodium bis(2-methoxyethoxy)aluminium dihydride; tris-(o-tolyl)phosphine; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole; In tetrahydrofuran; dichloromethane; water; acetonitrile; 5.1: Heck reaction;
DOI:10.1016/j.tetlet.2011.10.151
Guidance literature:
Multi-step reaction with 9 steps
1.1: mercury(II) diacetate / 36 h / Reflux
2.1: methylaluminium bis(4-bromo-2,6-di-tert.-butylphenoxide) / dichloromethane / 0.25 h / -78 °C
3.1: n-butyllithium / tetrahydrofuran
3.2: 2 h / -78 °C
4.1: Dess-Martin periodane / dichloromethane / 1 h / 0 °C
5.1: borane-THF; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole / tetrahydrofuran / 6 h / -40 °C
6.1: sodium bis(2-methoxyethoxy)aluminium dihydride / 4 h / 40 °C
6.2: 12 h / -78 - 0 °C
7.1: 2,6-dimethylpyridine / dichloromethane / 0.17 h / 20 °C
8.1: palladium diacetate; triethylamine; tris-(o-tolyl)phosphine / water; acetonitrile / 1.5 h / 80 °C
9.1: pyridine; pyridine hydrogenfluoride / tetrahydrofuran / 3 h / 40 °C
With pyridine; 2,6-dimethylpyridine; n-butyllithium; borane-THF; mercury(II) diacetate; palladium diacetate; Dess-Martin periodane; pyridine hydrogenfluoride; methylaluminium bis(4-bromo-2,6-di-tert.-butylphenoxide); triethylamine; sodium bis(2-methoxyethoxy)aluminium dihydride; tris-(o-tolyl)phosphine; (3aR)-1-methyl-3,3-diphenyl-tetrahydro-pyrrolo[1,2-c][1,3,2]oxazaborole; In tetrahydrofuran; dichloromethane; water; acetonitrile; 2.1: Claisen rearrangement / 8.1: Heck reaction;
DOI:10.1016/j.tetlet.2011.10.151
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