(E)-3-[(2-tert-butyldimethylsilyloxy)phenyl]-1-phenylprop-2-enol

Base Information

• Chemical Name: (E)-3-[(2-tert-butyldimethylsilyloxy)phenyl]-1-phenylprop-2-enol
• CAS No.: 514797-29-6
• Molecular Formula: C₂₁H₂₈O₂Si
• Molecular Weight: 340.538
• Mol file: 514797-29-6.mol

Synonyms:(E)-3-[(2-tert-butyldimethylsilyloxy)phenyl]-1-phenylprop-2-enol

Chemical Property of (E)-3-[(2-tert-butyldimethylsilyloxy)phenyl]-1-phenylprop-2-enol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (E)-3-[(2-tert-butyldimethylsilyloxy)phenyl]-1-phenylprop-2-enol

There total 6 articles about (E)-3-[(2-tert-butyldimethylsilyloxy)phenyl]-1-phenylprop-2-enol 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:

bromobenzene (108-86-1,52753-63-6) + (E)-3-[(2-tert-butyldimethylsilyloxy)phenyl]prop-2-enal (514797-26-3) → (E)-3-[(2-tert-butyldimethylsilyloxy)phenyl]-1-phenylprop-2-enol (514797-29-6)

Guidance literature:

bromobenzene; With magnesium; In diethyl ether;

(E)-3-[(2-tert-butyldimethylsilyloxy)phenyl]prop-2-enal; In diethyl ether; at 0 - 25 ℃;

DOI:10.1081/SCC-120014986

Reference yield:

tert-butyldimethylsilyl chloride (18162-48-6) → (E)-3-[(2-tert-butyldimethylsilyloxy)phenyl]-1-phenylprop-2-enol (514797-29-6)

Guidance literature:

Multi-step reaction with 2 steps

1.1: 64 percent / imidazole / dimethylformamide / 24 h / 25 °C

2.1: Mg / diethyl ether

2.2: diethyl ether / 0 - 25 °C

With 1H-imidazole; magnesium; In diethyl ether; N,N-dimethyl-formamide; 2.1: Grignard reaction / 2.2: Gignard reaction;

DOI:10.1081/SCC-120014986

Reference yield:

(E)-3-(2-hydroxyphenyl)propenal (60125-23-7) → (E)-3-[(2-tert-butyldimethylsilyloxy)phenyl]-1-phenylprop-2-enol (514797-29-6)

Guidance literature:

Multi-step reaction with 2 steps

1.1: 64 percent / imidazole / dimethylformamide / 24 h / 25 °C

2.1: Mg / diethyl ether

2.2: diethyl ether / 0 - 25 °C

With 1H-imidazole; magnesium; In diethyl ether; N,N-dimethyl-formamide; 2.1: Grignard reaction / 2.2: Gignard reaction;

DOI:10.1081/SCC-120014986

upstream raw materials:

bromobenzene

(E)-3-[(2-tert-butyldimethylsilyloxy)phenyl]prop-2-enal

(E)-3-(2-hydroxyphenyl)propenal

(E)-ethyl 2-hydroxycinnamate

Downstream raw materials:

acetic acid (E)-3-(2-hydroxyphenyl)-1-phenylprop-2-enol ester

2-phenylchromene

acetic acid (E)-3-[(2-tert-butyldimethylsilyloxy)phenyl]-1-phenylprop-2-enol ester