phenyl-(6-endo-phenyl-6-exo-pyridin-2-yl-bicyclo[2.1.1]hex-5-yl)-methanone

Base Information

Chemical Name:phenyl-(6-endo-phenyl-6-exo-pyridin-2-yl-bicyclo[2.1.1]hex-5-yl)-methanone
CAS No.:448211-11-8
Molecular Formula:C₂₄H₂₁NO
Molecular Weight:339.437
Hs Code.:

Synonyms:phenyl-(6-endo-phenyl-6-exo-pyridin-2-yl-bicyclo[2.1.1]hex-5-yl)-methanone

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of phenyl-(6-endo-phenyl-6-exo-pyridin-2-yl-bicyclo[2.1.1]hex-5-yl)-methanone

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Technology Process of phenyl-(6-endo-phenyl-6-exo-pyridin-2-yl-bicyclo[2.1.1]hex-5-yl)-methanone

There total 5 articles about phenyl-(6-endo-phenyl-6-exo-pyridin-2-yl-bicyclo[2.1.1]hex-5-yl)-methanone 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:

Reference yield: 40.0%

: 591-51-5
phenyllithium

: 490025-33-7
6-endo-phenyl-6-exo-pyridin-2-yl-bicyclo[2.1.1]hexane-5-carboxylic acid

: 448211-11-8
phenyl-(6-endo-phenyl-6-exo-pyridin-2-yl-bicyclo[2.1.1]hex-5-yl)-methanone

Guidance literature:: In diethyl ether; at 20 ℃; for 0.166667h;
DOI:10.1021/jo026187p

Reference yield:

: 2-{(1R,4S,5R)-6-[1-(tert-Butyl-dimethyl-silanyloxy)-1-phenyl-meth-(Z)-ylidene]-5-phenyl-bicyclo[2.1.1]hex-5-yl}-pyridine

: 448211-11-8
phenyl-(6-endo-phenyl-6-exo-pyridin-2-yl-bicyclo[2.1.1]hex-5-yl)-methanone

Guidance literature:: With hydrogenchloride; tetrabutyl ammonium fluoride; In acetonitrile; at 20 ℃; for 0.05h;
DOI:10.1021/jo026187p

Reference yield:

: 488862-90-4
(5-bromo-6-endo-phenyl-6-exo-pyridin-2-yl-bicyclo[2.1.1]hex-5-yl)-phenyl-methanone

: 448211-11-8
phenyl-(6-endo-phenyl-6-exo-pyridin-2-yl-bicyclo[2.1.1]hex-5-yl)-methanone

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / t-BuLi; HMPA / tetrahydrofuran / -78 - 20 °C

2: tetrabutylammonium fluoride; HCl / acetonitrile / 0.05 h / 20 °C

With hydrogenchloride; N,N,N,N,N,N-hexamethylphosphoric triamide; tetrabutyl ammonium fluoride; tert.-butyl lithium; In tetrahydrofuran; acetonitrile;
DOI:10.1021/jo026187p