acetic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester

Base Information

Chemical Name:acetic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester
CAS No.:1630974-77-4
Molecular Formula:C₁₇H₁₄N₂O₅
Molecular Weight:326.309
Hs Code.:

Synonyms:acetic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester

Suppliers and Price of acetic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of acetic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of acetic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester

There total 7 articles about acetic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl 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: 61.0%

: 1630974-74-1
2-(p-tolyl)-3-hydroxy-4-nitro-2,3-dihydroisoindol-1-one

: 75-36-5
acetyl chloride

: 1630974-77-4
acetic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester

Guidance literature:: With triethylamine; In acetonitrile; at 20 ℃; for 3h; Inert atmosphere;
DOI:10.5012/bkcs.2014.35.5.1337

Reference yield:

: 1630974-71-8
2-(p-tolyl)-4-nitro-2,3-dihydroisoindol-1-one

: 1630974-77-4
acetic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / acetonitrile / 2.5 h / 20 °C / Inert atmosphere; Reflux

2: triethylamine / acetonitrile / 3 h / 20 °C / Inert atmosphere

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); triethylamine; In acetonitrile;
DOI:10.5012/bkcs.2014.35.5.1337

Reference yield:

: 59382-59-1
2-methyl-3-nitro-benzoic acid methyl ester

: 1630974-77-4
acetic acid 7-nitro-3-oxo-2-(p-tolyl)-2,3-dihydro-1H-isoindol-1-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 26 h / 20 °C / Inert atmosphere; Reflux

2: potassium carbonate / acetonitrile / 5 h / 20 °C / Inert atmosphere

3: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / acetonitrile / 2.5 h / 20 °C / Inert atmosphere; Reflux

4: triethylamine / acetonitrile / 3 h / 20 °C / Inert atmosphere

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); potassium carbonate; triethylamine; In tetrachloromethane; acetonitrile;
DOI:10.5012/bkcs.2014.35.5.1337