6-tert-Butyl-3-{(Z)-2-[(2S,4R,6R)-4-(tert-butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-yl]-vinyl}-4-(4-fluoro-phenyl)-2-isopropyl-pyridine

Base Information

• Chemical Name: 6-tert-Butyl-3-{(Z)-2-[(2S,4R,6R)-4-(tert-butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-yl]-vinyl}-4-(4-fluoro-phenyl)-2-isopropyl-pyridine
• CAS No.: 122253-78-5
• Molecular Formula: C₄₂H₅₂FNO₃Si
• Molecular Weight: 665.964
• Mol file: 122253-78-5.mol

Synonyms:

Chemical Property of 6-tert-Butyl-3-{(Z)-2-[(2S,4R,6R)-4-(tert-butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-yl]-vinyl}-4-(4-fluoro-phenyl)-2-isopropyl-pyridine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 6-tert-Butyl-3-{(Z)-2-[(2S,4R,6R)-4-(tert-butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-yl]-vinyl}-4-(4-fluoro-phenyl)-2-isopropyl-pyridine

There total 7 articles about 6-tert-Butyl-3-{(Z)-2-[(2S,4R,6R)-4-(tert-butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-yl]-vinyl}-4-(4-fluoro-phenyl)-2-isopropyl-pyridine 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:

1-(4-fluorophenyl)-4,4-dimethylpent-1-en-3-one (80917-22-2) → 6-tert-Butyl-3-{(Z)-2-[(2S,4R,6R)-4-(tert-butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-yl]-vinyl}-4-(4-fluoro-phenyl)-2-isopropyl-pyridine (122253-78-5,123930-20-1)

Guidance literature:

Multi-step reaction with 6 steps

1: KOH, EtOH / diethyl ether / 3 h

2: ammonium acetate, FCl₃*6H₂O / acetic acid / 4 h / Heating

3: LiAlH₄ / tetrahydrofuran / 1.5 h / Ambient temperature

4: PBr₃ / toluene; CH₂Cl₂ / 1 h / Ambient temperature

5: toluene / 5 h / Heating

6: 1.) 1.6 M n-BuLi / 1.) THF, hexane, 0.5 h, 2.) 1 h

With ammonium acetate; potassium hydroxide; lithium aluminium tetrahydride; n-butyllithium; ethanol; phosphorus tribromide; In tetrahydrofuran; diethyl ether; dichloromethane; acetic acid; toluene;

DOI:10.1021/jm00163a010

Reference yield:

3-Bromomethyl-6-tert-butyl-4-(4-fluoro-phenyl)-2-isopropyl-pyridine (122253-36-5) → 6-tert-Butyl-3-{(Z)-2-[(2S,4R,6R)-4-(tert-butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-yl]-vinyl}-4-(4-fluoro-phenyl)-2-isopropyl-pyridine (122253-78-5,123930-20-1)

Guidance literature:

Multi-step reaction with 2 steps

1: toluene / 5 h / Heating

2: 1.) 1.6 M n-BuLi / 1.) THF, hexane, 0.5 h, 2.) 1 h

With n-butyllithium; In toluene;

DOI:10.1021/jm00163a010

Reference yield:

6-(1,1-Dimethylethyl)-4-(4-fluorophenyl)-2-(1-methylethyl)-3-pyridinemethanol (122253-13-8) → 6-tert-Butyl-3-{(Z)-2-[(2S,4R,6R)-4-(tert-butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-yl]-vinyl}-4-(4-fluoro-phenyl)-2-isopropyl-pyridine (122253-78-5,123930-20-1)

Guidance literature:

Multi-step reaction with 3 steps

1: PBr₃ / toluene; CH₂Cl₂ / 1 h / Ambient temperature

2: toluene / 5 h / Heating

3: 1.) 1.6 M n-BuLi / 1.) THF, hexane, 0.5 h, 2.) 1 h

With n-butyllithium; phosphorus tribromide; In dichloromethane; toluene;

DOI:10.1021/jm00163a010

upstream raw materials:

(2S,4R,6R)-4-(tert-Butyl-diphenyl-silanyloxy)-6-methoxy-tetrahydro-pyran-2-carbaldehyde

[6-tert-Butyl-4-(4-fluoro-phenyl)-2-isopropyl-pyridin-3-ylmethyl]-triphenyl-phosphonium; bromide

1-(4-fluorophenyl)-4,4-dimethylpent-1-en-3-one

6-(1,1-Dimethylethyl)-4-(4-fluorophenyl)-2-(1-methylethyl)-3-pyridinemethanol