2,6-di-t-butyl-4-dimethylamino-4-(3-phenylprop-2-ynyl)cyclohexa-2,5-dienone

Base Information

Chemical Name:2,6-di-t-butyl-4-dimethylamino-4-(3-phenylprop-2-ynyl)cyclohexa-2,5-dienone
CAS No.:50998-66-8
Molecular Formula:C₂₅H₃₃NO
Molecular Weight:363.543
Hs Code.:

Synonyms:2,6-di-t-butyl-4-dimethylamino-4-(3-phenylprop-2-ynyl)cyclohexa-2,5-dienone

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Chemical Property of 2,6-di-t-butyl-4-dimethylamino-4-(3-phenylprop-2-ynyl)cyclohexa-2,5-dienone

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Technology Process of 2,6-di-t-butyl-4-dimethylamino-4-(3-phenylprop-2-ynyl)cyclohexa-2,5-dienone

There total 3 articles about 2,6-di-t-butyl-4-dimethylamino-4-(3-phenylprop-2-ynyl)cyclohexa-2,5-dienone 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: 50.0%

: 50998-50-0
3,5-di-t-butyl-4-hydroxy-N,N-dimethyl-N-(3-phenylprop-2-ynyl)anilinium bromide

: 50998-64-6
2,6-di-t-butyl-4-dimethylamino-2-(3-phenylprop-2-ynyl)cyclohexa-3,5-dienone

: 50998-66-8
2,6-di-t-butyl-4-dimethylamino-4-(3-phenylprop-2-ynyl)cyclohexa-2,5-dienone

Guidance literature:: With sodium methylate; In methanol; at 0 ℃; for 20h; Title compound not separated from byproducts;

Reference yield:

: 10437-44-2
N,N-dimethyl-2,6-ditertiarybutyl-4-amino phenol

: 50998-66-8
2,6-di-t-butyl-4-dimethylamino-4-(3-phenylprop-2-ynyl)cyclohexa-2,5-dienone

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / acetonitrile

2: 50 percent / sodium methoxide / methanol / 20 h / 0 °C

With sodium methylate; In methanol; acetonitrile;

Reference yield:

: 1794-48-5
1-bromo-3-phenylprop-2-yne

: 50998-66-8
2,6-di-t-butyl-4-dimethylamino-4-(3-phenylprop-2-ynyl)cyclohexa-2,5-dienone

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / acetonitrile

2: 50 percent / sodium methoxide / methanol / 20 h / 0 °C

With sodium methylate; In methanol; acetonitrile;