2-(2-(5-methoxy)furanyl)-3-phenyl-1-pivaloylindoline

Base Information

Chemical Name:2-(2-(5-methoxy)furanyl)-3-phenyl-1-pivaloylindoline
CAS No.:87091-19-8
Molecular Formula:C₂₄H₂₅NO₃
Molecular Weight:375.467
Hs Code.:

Synonyms:2-(2-(5-methoxy)furanyl)-3-phenyl-1-pivaloylindoline

Suppliers and Price of 2-(2-(5-methoxy)furanyl)-3-phenyl-1-pivaloylindoline

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-(2-(5-methoxy)furanyl)-3-phenyl-1-pivaloylindoline

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-(2-(5-methoxy)furanyl)-3-phenyl-1-pivaloylindoline

There total 5 articles about 2-(2-(5-methoxy)furanyl)-3-phenyl-1-pivaloylindoline 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: 75.0%

: 87091-14-3,87143-98-4
1-(2-(5-methoxy)furanyl)-2-phenyl-2-(2-pivaloylamododiphenyl)ethanol

: 87091-19-8
2-(2-(5-methoxy)furanyl)-3-phenyl-1-pivaloylindoline

Guidance literature:: With dimethyl sulfoxide; triethylamine; trifluoroacetic anhydride; In dichloromethane; at -60 ℃; for 0.333333h;

Reference yield:

: 87091-05-2
2-hydroxymethyl-5-methoxy furan

: 87091-19-8
2-(2-(5-methoxy)furanyl)-3-phenyl-1-pivaloylindoline

Guidance literature:: Multi-step reaction with 3 steps

1: 69 percent / manganese dioxide / ethanol; CH₂Cl₂ / 16 h / Ambient temperature

2: 85 percent / n-BuLi, TMEDA / hexane; tetrahydrofuran / 1.) -30 deg C, 30 min, 2.) r.t., 1 h

3: 75 percent / trifluoroacetic anhydride, dimethyl sulfoxide, triethylamine / CH₂Cl₂ / 0.33 h / -60 °C

With manganese(IV) oxide; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; dimethyl sulfoxide; triethylamine; trifluoroacetic anhydride; In tetrahydrofuran; ethanol; hexane; dichloromethane;

Reference yield:

: 2527-99-3
methyl 5-bromo-2-furoate

: 87091-19-8
2-(2-(5-methoxy)furanyl)-3-phenyl-1-pivaloylindoline

Guidance literature:: Multi-step reaction with 5 steps

1: sodium iodide / methanol

2: 61 percent / lithium aluminium hydride

3: 69 percent / manganese dioxide / ethanol; CH₂Cl₂ / 16 h / Ambient temperature

4: 85 percent / n-BuLi, TMEDA / hexane; tetrahydrofuran / 1.) -30 deg C, 30 min, 2.) r.t., 1 h

5: 75 percent / trifluoroacetic anhydride, dimethyl sulfoxide, triethylamine / CH₂Cl₂ / 0.33 h / -60 °C

With manganese(IV) oxide; lithium aluminium tetrahydride; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; dimethyl sulfoxide; triethylamine; trifluoroacetic anhydride; sodium iodide; In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane;