2-[3-(4-Fluoro-phenyl)-1-hydroxy-2-isopropoxy-4-oxo-cyclobut-2-enyl]-4H-pyridine-1-carboxylic acid tert-butyl ester

Base Information

• Chemical Name: 2-[3-(4-Fluoro-phenyl)-1-hydroxy-2-isopropoxy-4-oxo-cyclobut-2-enyl]-4H-pyridine-1-carboxylic acid tert-butyl ester
• CAS No.: 1027902-15-3
• Molecular Formula: C₂₃H₂₆FNO₅
• Molecular Weight: 415.462
• Mol file: 1027902-15-3.mol

Synonyms:

Chemical Property of 2-[3-(4-Fluoro-phenyl)-1-hydroxy-2-isopropoxy-4-oxo-cyclobut-2-enyl]-4H-pyridine-1-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-[3-(4-Fluoro-phenyl)-1-hydroxy-2-isopropoxy-4-oxo-cyclobut-2-enyl]-4H-pyridine-1-carboxylic acid tert-butyl ester

There total 3 articles about 2-[3-(4-Fluoro-phenyl)-1-hydroxy-2-isopropoxy-4-oxo-cyclobut-2-enyl]-4H-pyridine-1-carboxylic acid tert-butyl 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:

pyridine (110-86-1) → 2-[3-(4-Fluoro-phenyl)-1-hydroxy-2-isopropoxy-4-oxo-cyclobut-2-enyl]-4H-pyridine-1-carboxylic acid tert-butyl ester (1027902-15-3)

Guidance literature:

Multi-step reaction with 3 steps

1: copper(I) iodide / tetrahydrofuran / 0.08 h

2: 1.) sodium borohydride / 2.) THF, room temperature

3: 1.) sec-butyllithium / 1.) THF, cyclohexane, -42 deg C, 3 h, 2.) THF, cyclohexane, -78 deg C

With sodium tetrahydroborate; copper(l) iodide; sec.-butyllithium; In tetrahydrofuran;

DOI:10.1021/jo970039v

Reference yield:

1-phenoxycarbonylpyridinium chloride (86801-40-3) → 2-[3-(4-Fluoro-phenyl)-1-hydroxy-2-isopropoxy-4-oxo-cyclobut-2-enyl]-4H-pyridine-1-carboxylic acid tert-butyl ester (1027902-15-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) sodium borohydride / 2.) THF, room temperature

2: 1.) sec-butyllithium / 1.) THF, cyclohexane, -42 deg C, 3 h, 2.) THF, cyclohexane, -78 deg C

With sodium tetrahydroborate; sec.-butyllithium;

DOI:10.1021/jo970039v

Reference yield:

tert-butyl pyridine-1(4H)-carboxylate (79329-06-9) + 4-(4-fluorophenyl)-3-isopropoxy-3-cyclobutene-1,2-dione → 2-[3-(4-Fluoro-phenyl)-1-hydroxy-2-isopropoxy-4-oxo-cyclobut-2-enyl]-4H-pyridine-1-carboxylic acid tert-butyl ester (1027902-15-3)

Guidance literature:

With sec.-butyllithium; Multistep reaction; 1.) THF, cyclohexane, -42 deg C, 3 h, 2.) THF, cyclohexane, -78 deg C;

DOI:10.1021/jo970039v

upstream raw materials:

tert-butyl pyridine-1(4H)-carboxylate

pyridine

1-phenoxycarbonylpyridinium chloride