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(3aS,7aS)-4,4,7a-trimethyloctahydro-1H-inden-1-one trisyl hydrazone

Base Information
  • Chemical Name:(3aS,7aS)-4,4,7a-trimethyloctahydro-1H-inden-1-one trisyl hydrazone
  • CAS No.:1379679-84-1
  • Molecular Formula:C27H44N2O2S
  • Molecular Weight:460.725
  • Hs Code.:
(3aS,7aS)-4,4,7a-trimethyloctahydro-1H-inden-1-one trisyl hydrazone

Synonyms:(3aS,7aS)-4,4,7a-trimethyloctahydro-1H-inden-1-one trisyl hydrazone

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Chemical Property of (3aS,7aS)-4,4,7a-trimethyloctahydro-1H-inden-1-one trisyl hydrazone
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Technology Process of (3aS,7aS)-4,4,7a-trimethyloctahydro-1H-inden-1-one trisyl hydrazone

There total 10 articles about (3aS,7aS)-4,4,7a-trimethyloctahydro-1H-inden-1-one trisyl hydrazone 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:
trisylhydrazine; (+)-(3aS,7aS)-4,4,7a-trimethyloctahydro-1H-inden-1-one; In acetonitrile; at 20 ℃; for 0.25h;
With tetrafluoroboric acid; In acetonitrile; at 20 ℃;
DOI:10.1002/ejoc.201200134
Guidance literature:
Multi-step reaction with 5 steps
1.1: n-butyllithium / hexane; tetrahydrofuran / -78 - 0 °C / Inert atmosphere
1.2: 16 h / -78 - 23 °C / Inert atmosphere
2.1: tetrabutyl ammonium fluoride / hexane; tetrahydrofuran / -78 - 23 °C / Inert atmosphere
3.1: n-butyllithium / hexane; tetrahydrofuran / 0.17 h / -78 - 0 °C / Inert atmosphere
3.2: 2 h / -78 - 23 °C / Inert atmosphere
4.1: tin(IV) chloride; (R)-3,3’-dichloro-1,1’-binaphthalene-2,2’-diol / dichloromethane / -78 °C / Inert atmosphere
4.2: 0 °C
5.1: tetrafluoroboric acid / acetonitrile / 14 h / 23 °C / Inert atmosphere
With (R)-3,3’-dichloro-1,1’-binaphthalene-2,2’-diol; tetrafluoroboric acid; n-butyllithium; tetrabutyl ammonium fluoride; tin(IV) chloride; In tetrahydrofuran; hexane; dichloromethane; acetonitrile;
DOI:10.1021/jacs.7b13799
Guidance literature:
Multi-step reaction with 3 steps
1.1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 16 h / 7600.51 Torr
2.1: dimethylsulfide borane complex; (S)-1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole / tetrahydrofuran / 0.28 h / 0 °C
2.2: 1 h / 0 - 20 °C
3.1: acetonitrile / 0.25 h / 20 °C
3.2: 20 °C
With dimethylsulfide borane complex; palladium 10% on activated carbon; hydrogen; (S)-1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole; In tetrahydrofuran; ethyl acetate; acetonitrile;
DOI:10.1002/ejoc.201200134
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