N-[2-(4-tert-butyl-benzoyl)-phenyl]-2-(4-tert-butyl-phenyl)-4-oxo-4-(2,4,6-trimethyl-phenyl)-butyramide

Base Information

Chemical Name:N-[2-(4-tert-butyl-benzoyl)-phenyl]-2-(4-tert-butyl-phenyl)-4-oxo-4-(2,4,6-trimethyl-phenyl)-butyramide
CAS No.:234103-87-8
Molecular Formula:C₄₀H₄₅NO₃
Molecular Weight:587.802
Hs Code.:

<i>N</i>-[2-(4-<i>tert</i>-butyl-benzoyl)-phenyl]-2-(4-<i>tert</i>-butyl-phenyl)-4-oxo-4-(2,4,6-trimethyl-phenyl)-butyramide

Synonyms:N-[2-(4-tert-butyl-benzoyl)-phenyl]-2-(4-tert-butyl-phenyl)-4-oxo-4-(2,4,6-trimethyl-phenyl)-butyramide

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Chemical Property of N-[2-(4-tert-butyl-benzoyl)-phenyl]-2-(4-tert-butyl-phenyl)-4-oxo-4-(2,4,6-trimethyl-phenyl)-butyramide

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Technology Process of N-[2-(4-tert-butyl-benzoyl)-phenyl]-2-(4-tert-butyl-phenyl)-4-oxo-4-(2,4,6-trimethyl-phenyl)-butyramide

There total 4 articles about N-[2-(4-tert-butyl-benzoyl)-phenyl]-2-(4-tert-butyl-phenyl)-4-oxo-4-(2,4,6-trimethyl-phenyl)-butyramide 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: 85.0%

: 253185-03-4,253185-04-5
tert-butylbenzene

: 234103-30-1
2-[2-(2,4,6-trimethylbenzoyl)vinyl]-4H-3,1-benzoxazin-4-one

: 234103-87-8
N-[2-(4-tert-butyl-benzoyl)-phenyl]-2-(4-tert-butyl-phenyl)-4-oxo-4-(2,4,6-trimethyl-phenyl)-butyramide

Guidance literature:: With hydrogenchloride; aluminium trichloride; In 1,1,2,2-tetrachloroethane; for 4h;

Reference yield:

: 22660-12-4
β-(2,4,6-trimethylbenzoyl)acrylic acid

: 234103-87-8
N-[2-(4-tert-butyl-benzoyl)-phenyl]-2-(4-tert-butyl-phenyl)-4-oxo-4-(2,4,6-trimethyl-phenyl)-butyramide

Guidance literature:: Multi-step reaction with 4 steps

1: PCl₅

2: 60 percent / diethyl ether

3: 94 percent / Ac₂O / 3 h / Heating

4: 85 percent / HCl; AlCl₃ / 1,1,2,2-tetrachloro-ethane / 4 h

With hydrogenchloride; aluminium trichloride; phosphorus pentachloride; acetic anhydride; In diethyl ether; 1,1,2,2-tetrachloroethane; 1: Chlorination / 2: Condensation / 3: Cyclization / 4: Condensation;

Reference yield:

: 234103-26-5
β-(2,4,6-trimethylbenzoyl)acryloyl chloride

: 234103-87-8
N-[2-(4-tert-butyl-benzoyl)-phenyl]-2-(4-tert-butyl-phenyl)-4-oxo-4-(2,4,6-trimethyl-phenyl)-butyramide

Guidance literature:: Multi-step reaction with 3 steps

1: 60 percent / diethyl ether

2: 94 percent / Ac₂O / 3 h / Heating

3: 85 percent / HCl; AlCl₃ / 1,1,2,2-tetrachloro-ethane / 4 h

With hydrogenchloride; aluminium trichloride; acetic anhydride; In diethyl ether; 1,1,2,2-tetrachloroethane; 1: Condensation / 2: Cyclization / 3: Condensation;