2-Naphthalenamine, 8-bromo-1,2,3,4-tetrahydro-5-methyl-N-(phenylmethyl)-

Base Information

Chemical Name:2-Naphthalenamine, 8-bromo-1,2,3,4-tetrahydro-5-methyl-N-(phenylmethyl)-
CAS No.:633312-83-1
Molecular Formula:C18H20BrN
Molecular Weight:
Hs Code.:

Synonyms:

Suppliers and Price of 2-Naphthalenamine, 8-bromo-1,2,3,4-tetrahydro-5-methyl-N-(phenylmethyl)-

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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-Naphthalenamine, 8-bromo-1,2,3,4-tetrahydro-5-methyl-N-(phenylmethyl)-

Chemical Property:

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Technology Process of 2-Naphthalenamine, 8-bromo-1,2,3,4-tetrahydro-5-methyl-N-(phenylmethyl)-

There total 4 articles about 2-Naphthalenamine, 8-bromo-1,2,3,4-tetrahydro-5-methyl-N-(phenylmethyl)- 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:

: 621-36-3
m-methylphenylacetic acid

: 633312-83-1
C₁₈H₂₀BrN

Guidance literature:: Multi-step reaction with 4 steps

1: bromine; potassium carbonate / water

2: thionyl chloride / dichloromethane / 30 °C / Reflux

3: aluminum (III) chloride

4: sodium tris(acetoxy)borohydride

With aluminum (III) chloride; thionyl chloride; bromine; sodium tris(acetoxy)borohydride; potassium carbonate; In dichloromethane; water; 3: Friedel Crafts alkylation;
DOI:10.1021/jo300277y

Reference yield:

: 203314-29-8
2-bromo-5-methylphenylacetic acid

: 633312-83-1
C₁₈H₂₀BrN

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride / dichloromethane / 30 °C / Reflux

2: aluminum (III) chloride

3: sodium tris(acetoxy)borohydride

With aluminum (III) chloride; thionyl chloride; sodium tris(acetoxy)borohydride; In dichloromethane; 2: Friedel Crafts alkylation;
DOI:10.1021/jo300277y

Reference yield:

: C₉H₈BrClO

: 633312-83-1
C₁₈H₂₀BrN

Guidance literature:: Multi-step reaction with 2 steps

1: aluminum (III) chloride

2: sodium tris(acetoxy)borohydride

With aluminum (III) chloride; sodium tris(acetoxy)borohydride; 1: Friedel Crafts alkylation;
DOI:10.1021/jo300277y