r-2-Ethoxy-t-3-hydroxy-1-methyl-3-phenyl-2-<(p-trifluormethyl)phenyl>indolin

Base Information

Chemical Name:r-2-Ethoxy-t-3-hydroxy-1-methyl-3-phenyl-2-<(p-trifluormethyl)phenyl>indolin
CAS No.:86839-48-7
Molecular Formula:C₂₄H₂₂F₃NO₂
Molecular Weight:413.439
Hs Code.:

Synonyms:r-2-Ethoxy-t-3-hydroxy-1-methyl-3-phenyl-2-<(p-trifluormethyl)phenyl>indolin

Suppliers and Price of r-2-Ethoxy-t-3-hydroxy-1-methyl-3-phenyl-2-<(p-trifluormethyl)phenyl>indolin

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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 r-2-Ethoxy-t-3-hydroxy-1-methyl-3-phenyl-2-<(p-trifluormethyl)phenyl>indolin

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Technology Process of r-2-Ethoxy-t-3-hydroxy-1-methyl-3-phenyl-2-<(p-trifluormethyl)phenyl>indolin

There total 5 articles about r-2-Ethoxy-t-3-hydroxy-1-methyl-3-phenyl-2-<(p-trifluormethyl)phenyl>indolin 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: 58.0%

: 86839-41-0
2-Ethoxy-1-methyl-4-phenyl-2-<(p-trifluormethyl)phenyl>-1,2-dihydro-4H-3,1-benzoxazin

: 86839-48-7
r-2-Ethoxy-t-3-hydroxy-1-methyl-3-phenyl-2-<(p-trifluormethyl)phenyl>indolin

Guidance literature:: With n-butyllithium; In tetrahydrofuran; hexane; at -80 ℃;

Reference yield:

: 86839-21-6
4-Phenyl-2-<(p-trifuormethyl)phenyl>-4H-3,1-benzoxazin

: 86839-48-7
r-2-Ethoxy-t-3-hydroxy-1-methyl-3-phenyl-2-<(p-trifluormethyl)phenyl>indolin

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / CH₂Cl₂ / 12 h / Ambient temperature

2: 84 percent / 0 °C

3: 58 percent / BuLi / tetrahydrofuran; hexane / -80 °C

With n-butyllithium; In tetrahydrofuran; hexane; dichloromethane;

Reference yield:

: 86839-12-5
2-<(p-Trifluormethyl)benzoylamino>benzophenon

: 86839-48-7
r-2-Ethoxy-t-3-hydroxy-1-methyl-3-phenyl-2-<(p-trifluormethyl)phenyl>indolin

Guidance literature:: Multi-step reaction with 5 steps

1: 97 percent / NaBH₄

2: 70 percent / PBr₃ / CH₂Cl₂

3: 90 percent / CH₂Cl₂ / 12 h / Ambient temperature

4: 84 percent / 0 °C

5: 58 percent / BuLi / tetrahydrofuran; hexane / -80 °C

With sodium tetrahydroborate; n-butyllithium; phosphorus tribromide; In tetrahydrofuran; hexane; dichloromethane;