2-((2R,3R)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione

Base Information

Chemical Name:2-((2R,3R)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione
CAS No.:1643786-42-8
Molecular Formula:C₂₃H₁₈N₂O₂
Molecular Weight:354.408
Hs Code.:

Synonyms:2-((2R,3R)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione

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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-((2R,3R)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione

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Technology Process of 2-((2R,3R)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione

There total 4 articles about 2-((2R,3R)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione 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: 83.0%

: 1643786-42-8
2-((2R,3R)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione

: 1620395-12-1
2-((S,3S)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione

Guidance literature:: With palladium(II) trifluoroacetate; C₄₂H₂₈O₁₂P₂; hydrogen; trifluoroacetic acid; In dichloromethane; at 70 ℃; for 18h; under 51716.2 Torr; enantioselective reaction; Glovebox; Autoclave;

Reference yield:

: 102594-89-8
2-(2-phenylquinolin-3-yl)isoindoline-1,3-dione

: 1643786-42-8
2-((2R,3R)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione

: 1620395-12-1
2-((S,3S)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione

Guidance literature:: With (R)-(-)-5,5’-bis(diphenyl;phosphine)-2,2,2’,2’-tetrafluoro-4,4’-bi-1,3-benzodioxole; bis(1,5-cyclooctadiene)diiridium(I) dichloride; hydrogen; iodine; In tetrahydrofuran; toluene; at 70 ℃; for 18h; under 10343.2 Torr; Overall yield = 97 %; enantioselective reaction; Inert atmosphere; Glovebox; Autoclave;
DOI:10.1002/chem.201402592

Reference yield:

: 5443-79-8
3-nitro-2-phenylquinoline

: 1643786-42-8
2-((2R,3R)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione

: 1620395-12-1
2-((S,3S)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione

Guidance literature:: Multi-step reaction with 3 steps

1: iron; hydrogenchloride / water; ethanol / 85 °C

2: acetic acid / 18 h / 120 °C

3: bis(1,5-cyclooctadiene)diiridium(I) dichloride; iodine; hydrogen; (R)-(-)-5,5’-bis(diphenyl;phosphine)-2,2,2’,2’-tetrafluoro-4,4’-bi-1,3-benzodioxole / tetrahydrofuran; toluene / 18 h / 70 °C / 10343.2 Torr / Inert atmosphere; Glovebox; Autoclave

With (R)-(-)-5,5’-bis(diphenyl;phosphine)-2,2,2’,2’-tetrafluoro-4,4’-bi-1,3-benzodioxole; hydrogenchloride; bis(1,5-cyclooctadiene)diiridium(I) dichloride; hydrogen; iodine; iron; acetic acid; In tetrahydrofuran; ethanol; water; toluene;
DOI:10.1002/chem.201402592