2--1-benzoylnaphthalene

Base Information

Chemical Name:2--1-benzoylnaphthalene
CAS No.:154848-96-1
Molecular Formula:C₁₉H₁₄BrNO₂
Molecular Weight:368.23
Hs Code.:

2-<N-(bromoacetyl)amino>-1-benzoylnaphthalene

Synonyms:2--1-benzoylnaphthalene

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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 2--1-benzoylnaphthalene

Chemical Property:

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Technology Process of 2--1-benzoylnaphthalene

There total 3 articles about 2--1-benzoylnaphthalene 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: 89.0%

: 116400-82-9
2-amino-1-benzoylnaphthalene

: 598-21-0
2-Bromoacetyl bromide

: 154848-96-1
2--1-benzoylnaphthalene

Guidance literature:: With sodium hydrogencarbonate; In chloroform; at 0 ℃; for 0.5h;
DOI:10.1021/jm00032a007

Reference yield:

: 7066-13-9
2-aminonaphthalene-1-carbonitrile

: 154848-96-1
2--1-benzoylnaphthalene

Guidance literature:: Multi-step reaction with 2 steps

1: 2.) 6 N aq. HCl / 1.) Et₂O, reflux, 1 h, 2.) Et₂O, 30 deg C, 5 h

2: 89 percent / NaHCO₃ / CHCl₃ / 0.5 h / 0 °C

With hydrogenchloride; sodium hydrogencarbonate; In chloroform;
DOI:10.1021/jm00032a007

Reference yield:

: phenylmagnesium bromide

: 154848-96-1
2--1-benzoylnaphthalene

Guidance literature:: Multi-step reaction with 2 steps

1: 2.) 6 N aq. HCl / 1.) Et₂O, reflux, 1 h, 2.) Et₂O, 30 deg C, 5 h

2: 89 percent / NaHCO₃ / CHCl₃ / 0.5 h / 0 °C

With hydrogenchloride; sodium hydrogencarbonate; In chloroform;
DOI:10.1021/jm00032a007