rac-trans-1-benzoyl-5-benzyl-2-(tert-butyl)tetrahydro-3-methylpyrimidin-4(1H)-one

Base Information

Chemical Name:rac-trans-1-benzoyl-5-benzyl-2-(tert-butyl)tetrahydro-3-methylpyrimidin-4(1H)-one
CAS No.:131932-59-7
Molecular Formula:C₂₃H₂₈N₂O₂
Molecular Weight:364.488
Hs Code.:

Synonyms:rac-trans-1-benzoyl-5-benzyl-2-(tert-butyl)tetrahydro-3-methylpyrimidin-4(1H)-one

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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 rac-trans-1-benzoyl-5-benzyl-2-(tert-butyl)tetrahydro-3-methylpyrimidin-4(1H)-one

Chemical Property:

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MSDS Files:: SDS file from LookChem

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Technology Process of rac-trans-1-benzoyl-5-benzyl-2-(tert-butyl)tetrahydro-3-methylpyrimidin-4(1H)-one

There total 2 articles about rac-trans-1-benzoyl-5-benzyl-2-(tert-butyl)tetrahydro-3-methylpyrimidin-4(1H)-one 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:

: 131932-57-5
β--N-methyl-propionamide

: 131932-59-7
rac-trans-1-benzoyl-5-benzyl-2-(tert-butyl)tetrahydro-3-methylpyrimidin-4(1H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / 9 h / 180 °C

2: 1) LDA / 1) THF, -75 deg C, 45 min, 2) 30 min, room temperature, THF

With lithium diisopropyl amide;
DOI:10.1021/jo00007a053

Reference yield:

: 100-39-0
benzyl bromide

: 131932-56-4
rac-1-benzoyl-2-(tert-butyl)tetrahydro-3-methylpyrimidin-4(1H)-one

: 131932-59-7
rac-trans-1-benzoyl-5-benzyl-2-(tert-butyl)tetrahydro-3-methylpyrimidin-4(1H)-one

Guidance literature:: With lithium diisopropyl amide; Yield given. Multistep reaction; 1) THF, -75 deg C, 45 min, 2) 30 min, room temperature, THF;
DOI:10.1021/jo00007a053