7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-naphthalen-1-yl-2H-chromene

Base Information

• Chemical Name: 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-naphthalen-1-yl-2H-chromene
• CAS No.: 173676-38-5
• Molecular Formula: C₃₇H₄₆O₃Si₂
• Molecular Weight: 594.941
• Mol file: 173676-38-5.mol

Synonyms:7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-naphthalen-1-yl-2H-chromene

Chemical Property of 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-naphthalen-1-yl-2H-chromene

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-naphthalen-1-yl-2H-chromene

There total 5 articles about 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-naphthalen-1-yl-2H-chromene 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: 70.0%

1-naphthylmagnesiumbromide (703-55-9) + 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-phenoxy-2H-chromene (173676-53-4) → 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-naphthalen-1-yl-2H-chromene (173676-38-5)

Guidance literature:

In toluene; 0 deg C to RT;

DOI:10.1016/0040-4039(95)01916-6

Reference yield:

7-methoxy-3-(4-methoxyphenyl)-2H-chromen-2-one (3173-00-0) → 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-naphthalen-1-yl-2H-chromene (173676-38-5)

Guidance literature:

Multi-step reaction with 4 steps

1: 1.) EtSH, AlCl₃, 2.) Et₃N / 1.) CH₂Cl₂, 2.) CH₂Cl₂

2: 83 percent / DIBAL-H / toluene / -78 °C

3: 97 percent / chlorobenzene / Heating

4: 70 percent / toluene / 0 deg C to RT

With aluminium trichloride; diisobutylaluminium hydride; triethylamine; ethanethiol; In chlorobenzene; toluene;

DOI:10.1016/0040-4039(95)01916-6

Reference yield:

tert-butyldimethylsilyl chloride (18162-48-6) → 7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-naphthalen-1-yl-2H-chromene (173676-38-5)

Guidance literature:

Multi-step reaction with 4 steps

1: 1.) EtSH, AlCl₃, 2.) Et₃N / 1.) CH₂Cl₂, 2.) CH₂Cl₂

2: 83 percent / DIBAL-H / toluene / -78 °C

3: 97 percent / chlorobenzene / Heating

4: 70 percent / toluene / 0 deg C to RT

With aluminium trichloride; diisobutylaluminium hydride; triethylamine; ethanethiol; In chlorobenzene; toluene;

DOI:10.1016/0040-4039(95)01916-6

upstream raw materials:

1-naphthylmagnesiumbromide

7-(tert-Butyl-dimethyl-silanyloxy)-3-[4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-2-phenoxy-2H-chromene

7-methoxy-3-(4-methoxyphenyl)-2H-chromen-2-one

tert-butyldimethylsilyl chloride