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(S)-ethyl 2-(dibenzylamino)-2-[(1,3-dioxoisoindolin-2-yl)methyl]propanoate

Base Information Edit
  • Chemical Name:(S)-ethyl 2-(dibenzylamino)-2-[(1,3-dioxoisoindolin-2-yl)methyl]propanoate
  • CAS No.:1453178-67-0
  • Molecular Formula:C28H28N2O4
  • Molecular Weight:456.541
  • Hs Code.:
  • Mol file:1453178-67-0.mol
(S)-ethyl 2-(dibenzylamino)-2-[(1,3-dioxoisoindolin-2-yl)methyl]propanoate

Synonyms:(S)-ethyl 2-(dibenzylamino)-2-[(1,3-dioxoisoindolin-2-yl)methyl]propanoate

Suppliers and Price of (S)-ethyl 2-(dibenzylamino)-2-[(1,3-dioxoisoindolin-2-yl)methyl]propanoate
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Chemical Property of (S)-ethyl 2-(dibenzylamino)-2-[(1,3-dioxoisoindolin-2-yl)methyl]propanoate Edit
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Technology Process of (S)-ethyl 2-(dibenzylamino)-2-[(1,3-dioxoisoindolin-2-yl)methyl]propanoate

There total 5 articles about (S)-ethyl 2-(dibenzylamino)-2-[(1,3-dioxoisoindolin-2-yl)methyl]propanoate 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:
Guidance literature:
Multi-step reaction with 5 steps
1.1: sodium hydride / mineral oil; tetrahydrofuran / 1.5 h / 0 - 20 °C
1.2: 12 h / Reflux
2.1: pig liver esterase / aq. phosphate buffer; ethanol / pH 7.4 / Enzymatic reaction
3.1: triethylamine; diphenyl phosphoryl azide / 1,2-dichloro-ethane / 3.5 h / 20 °C / Inert atmosphere; Reflux
3.2: 12 h / Reflux; Inert atmosphere
4.1: trifluoroacetic acid / dichloromethane / 1 h
5.1: potassium carbonate / acetonitrile / 12 h / Inert atmosphere; Reflux
With pig liver esterase; diphenyl phosphoryl azide; sodium hydride; potassium carbonate; triethylamine; trifluoroacetic acid; In tetrahydrofuran; aq. phosphate buffer; ethanol; dichloromethane; 1,2-dichloro-ethane; acetonitrile; mineral oil; 3.2: |Curtius Rearrangement;
DOI:10.1039/c3ob41282b
Guidance literature:
Multi-step reaction with 5 steps
1.1: sodium hydride / mineral oil; tetrahydrofuran / 1.5 h / 0 - 20 °C
1.2: 12 h / Reflux
2.1: pig liver esterase / aq. phosphate buffer; ethanol / pH 7.4 / Enzymatic reaction
3.1: triethylamine; diphenyl phosphoryl azide / 1,2-dichloro-ethane / 3.5 h / 20 °C / Inert atmosphere; Reflux
3.2: 12 h / Reflux; Inert atmosphere
4.1: trifluoroacetic acid / dichloromethane / 1 h
5.1: potassium carbonate / acetonitrile / 12 h / Inert atmosphere; Reflux
With pig liver esterase; diphenyl phosphoryl azide; sodium hydride; potassium carbonate; triethylamine; trifluoroacetic acid; In tetrahydrofuran; aq. phosphate buffer; ethanol; dichloromethane; 1,2-dichloro-ethane; acetonitrile; mineral oil; 3.2: |Curtius Rearrangement;
DOI:10.1039/c3ob41282b
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