4-Nitro-benzoic acid 1-(2,2-dimethyl-propyl)-3,3-dimethyl-1-phenyl-butyl ester

Base Information

• Chemical Name: 4-Nitro-benzoic acid 1-(2,2-dimethyl-propyl)-3,3-dimethyl-1-phenyl-butyl ester
• CAS No.: 40543-96-2
• Molecular Formula: C₂₄H₃₁NO₄
• Molecular Weight: 397.514

Synonyms:4-Nitro-benzoic acid 1-(2,2-dimethyl-propyl)-3,3-dimethyl-1-phenyl-butyl ester

Chemical Property of 4-Nitro-benzoic acid 1-(2,2-dimethyl-propyl)-3,3-dimethyl-1-phenyl-butyl ester

Chemical Property:

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Technology Process of 4-Nitro-benzoic acid 1-(2,2-dimethyl-propyl)-3,3-dimethyl-1-phenyl-butyl ester

There total 1 articles about 4-Nitro-benzoic acid 1-(2,2-dimethyl-propyl)-3,3-dimethyl-1-phenyl-butyl ester 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:

bromobenzene (108-86-1,52753-63-6) + dineopentyl ketone (4436-99-1) + 4-nitro-benzoyl chloride (122-04-3) → 4-Nitro-benzoic acid 1-(2,2-dimethyl-propyl)-3,3-dimethyl-1-phenyl-butyl ester (40543-96-2)

Guidance literature:

Multistep reaction; (i) Li, Et₂O, (ii) /BRN= 1753187/, (iii) /BRN= 473192/;

DOI:10.1021/ja00786a038

Reference yield:

4-Nitro-benzoic acid 1-(2,2-dimethyl-propyl)-3,3-dimethyl-1-phenyl-butyl ester (40543-96-2) → 4-Phenyl-2,2,6,6-tetramethylheptan (40544-17-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 200 °C

2: H₂ / Pd-C / ethanol

With hydrogen; palladium on activated charcoal; In ethanol;

DOI:10.1021/ja00786a038

Reference yield:

4-Nitro-benzoic acid 1-(2,2-dimethyl-propyl)-3,3-dimethyl-1-phenyl-butyl ester (40543-96-2) → [(Z)-1-(2,2-Dimethyl-propyl)-3,3-dimethyl-but-1-enyl]-benzene

Guidance literature:

at 200 ℃;

DOI:10.1021/ja00786a038

upstream raw materials:

bromobenzene

dineopentyl ketone

4-nitro-benzoyl chloride

Downstream raw materials:

4-Phenyl-2,2,6,6-tetramethylheptan

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