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rel-(4aS,8aS)-8a-<(benzyloxy)methyl>-1,4,4a,5,6,7,8,8a-octahydro-2(3H)-naphthalenone

Base Information Edit
  • Chemical Name:rel-(4aS,8aS)-8a-<(benzyloxy)methyl>-1,4,4a,5,6,7,8,8a-octahydro-2(3H)-naphthalenone
  • CAS No.:108743-95-9
  • Molecular Formula:C18H24O2
  • Molecular Weight:272.387
  • Hs Code.:
  • Mol file:108743-95-9.mol
rel-(4aS,8aS)-8a-<(benzyloxy)methyl>-1,4,4a,5,6,7,8,8a-octahydro-2(3H)-naphthalenone

Synonyms:rel-(4aS,8aS)-8a-<(benzyloxy)methyl>-1,4,4a,5,6,7,8,8a-octahydro-2(3H)-naphthalenone

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Chemical Property of rel-(4aS,8aS)-8a-<(benzyloxy)methyl>-1,4,4a,5,6,7,8,8a-octahydro-2(3H)-naphthalenone Edit
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Technology Process of rel-(4aS,8aS)-8a-<(benzyloxy)methyl>-1,4,4a,5,6,7,8,8a-octahydro-2(3H)-naphthalenone

There total 2 articles about rel-(4aS,8aS)-8a-<(benzyloxy)methyl>-1,4,4a,5,6,7,8,8a-octahydro-2(3H)-naphthalenone 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:
Multi-step reaction with 2 steps
1: 1.) NaH, 2.) n-BuLi / 1.) THF, DMF, 2.) THF, Et2O, -78 deg C, 50 min
2: 1.) n-butyllithium, 2.) copper(I)bromide-dimethyl sulfide complex 3.) chlorotrimethylsilane / 2.) isopropylmagnesium chloride / 1.) hexane, -78 deg C, 10 min, 2.) diisopropyl sulfide, THF, -78 deg C, 15 min, 3.) THF, diisopropyl sulfide, hexane, -78 deg C, 15 min, - 40 deg C, 10 min, 0 deg C, 2 min
With n-butyllithium; chloro-trimethyl-silane; copper(I) bromide dimethylsulfide complex; sodium hydride; isopropylmagnesium chloride;
DOI:10.1021/ja00250a029
Guidance literature:
With n-butyllithium; chloro-trimethyl-silane; copper(I) bromide dimethylsulfide complex; isopropylmagnesium chloride; Yield given. Multistep reaction; 1.) hexane, -78 deg C, 10 min, 2.) diisopropyl sulfide, THF, -78 deg C, 15 min, 3.) THF, diisopropyl sulfide, hexane, -78 deg C, 15 min, - 40 deg C, 10 min, 0 deg C, 2 min;
DOI:10.1021/ja00250a029
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