N-(5-bromo-2-(3-(4-chlorophenyl)prop-2-ynyloxy)benzylidene)tert-butylamine

Base Information

Chemical Name:N-(5-bromo-2-(3-(4-chlorophenyl)prop-2-ynyloxy)benzylidene)tert-butylamine
CAS No.:1610629-06-5
Molecular Formula:C₂₀H₁₉BrClNO
Molecular Weight:404.734
Hs Code.:

Synonyms:N-(5-bromo-2-(3-(4-chlorophenyl)prop-2-ynyloxy)benzylidene)tert-butylamine

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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 N-(5-bromo-2-(3-(4-chlorophenyl)prop-2-ynyloxy)benzylidene)tert-butylamine

Chemical Property:

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Technology Process of N-(5-bromo-2-(3-(4-chlorophenyl)prop-2-ynyloxy)benzylidene)tert-butylamine

There total 3 articles about N-(5-bromo-2-(3-(4-chlorophenyl)prop-2-ynyloxy)benzylidene)tert-butylamine 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:

: 1610629-40-7
C₁₆H₁₀BrClO₂

: 75-64-9
tert-butylamine

: 1610629-06-5
N-(5-bromo-2-(3-(4-chlorophenyl)prop-2-ynyloxy)benzylidene)tert-butylamine

Guidance literature:: In neat (no solvent); at 20 ℃; for 24h;
DOI:10.1016/j.tet.2014.04.053

Reference yield:

: 173019-82-4
1-(3-bromo-prop-1-ynyl)-4-chloro-benzene

: 1610629-06-5
N-(5-bromo-2-(3-(4-chlorophenyl)prop-2-ynyloxy)benzylidene)tert-butylamine

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 4 h / 80 °C

2: neat (no solvent) / 24 h / 20 °C

With potassium carbonate; In acetonitrile;
DOI:10.1016/j.tet.2014.04.053

Reference yield:

: 1761-61-1
5-bromosalicyclaldehyde

: 1610629-06-5
N-(5-bromo-2-(3-(4-chlorophenyl)prop-2-ynyloxy)benzylidene)tert-butylamine

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 4 h / 80 °C

2: neat (no solvent) / 24 h / 20 °C

With potassium carbonate; In acetonitrile;
DOI:10.1016/j.tet.2014.04.053