1-{2-[2-{2-[2-(4-methylphenylsulfonyloxy)ethoxy]ethoxy}ethoxy]ethoxy}-4-{2-[2-{2-[2-(4-triphenylmethylphenoxy)ethoxy]ethoxy}ethoxy]ethoxy}benzene

Base Information

Chemical Name:1-{2-[2-{2-[2-(4-methylphenylsulfonyloxy)ethoxy]ethoxy}ethoxy]ethoxy}-4-{2-[2-{2-[2-(4-triphenylmethylphenoxy)ethoxy]ethoxy}ethoxy]ethoxy}benzene
CAS No.:264124-15-4
Molecular Formula:C₅₄H₆₂O₁₂S
Molecular Weight:935.145
Hs Code.:

Synonyms:1-{2-[2-{2-[2-(4-methylphenylsulfonyloxy)ethoxy]ethoxy}ethoxy]ethoxy}-4-{2-[2-{2-[2-(4-triphenylmethylphenoxy)ethoxy]ethoxy}ethoxy]ethoxy}benzene

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Chemical Property of 1-{2-[2-{2-[2-(4-methylphenylsulfonyloxy)ethoxy]ethoxy}ethoxy]ethoxy}-4-{2-[2-{2-[2-(4-triphenylmethylphenoxy)ethoxy]ethoxy}ethoxy]ethoxy}benzene

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Technology Process of 1-{2-[2-{2-[2-(4-methylphenylsulfonyloxy)ethoxy]ethoxy}ethoxy]ethoxy}-4-{2-[2-{2-[2-(4-triphenylmethylphenoxy)ethoxy]ethoxy}ethoxy]ethoxy}benzene

There total 7 articles about 1-{2-[2-{2-[2-(4-methylphenylsulfonyloxy)ethoxy]ethoxy}ethoxy]ethoxy}-4-{2-[2-{2-[2-(4-triphenylmethylphenoxy)ethoxy]ethoxy}ethoxy]ethoxy}benzene 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:

: 77544-60-6
p-toluenesulfonic acid 2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethyl ester

: 264124-15-4
1-{2-[2-{2-[2-(4-methylphenylsulfonyloxy)ethoxy]ethoxy}ethoxy]ethoxy}-4-{2-[2-{2-[2-(4-triphenylmethylphenoxy)ethoxy]ethoxy}ethoxy]ethoxy}benzene

Guidance literature:: Multi-step reaction with 4 steps

1: 74 percent / K₂CO₃ / dimethylformamide / 10 h / 80 °C

2: H₂ / 10percent Pd/C / methanol; CH₂Cl₂ / 5 h / 20 °C

3: 65 percent / K₂CO₃ / dimethylformamide / 168 h / 80 °C

4: 88 percent / Et₃N; DMAP / CH₂Cl₂ / 2 h / 20 °C

With dmap; hydrogen; potassium carbonate; triethylamine; 10percent Pd/C; In methanol; dichloromethane; N,N-dimethyl-formamide; 1: Alkylation / 2: Hydrogenolysis / 3: Alkylation / 4: Tosylation;
DOI:10.1002/(SICI)1099-0690(200002)2000:4<591::AID-EJOC591>3.0.CO;2-I

Reference yield:

: 103-16-2
4-Benzyloxyphenol

: 264124-15-4
1-{2-[2-{2-[2-(4-methylphenylsulfonyloxy)ethoxy]ethoxy}ethoxy]ethoxy}-4-{2-[2-{2-[2-(4-triphenylmethylphenoxy)ethoxy]ethoxy}ethoxy]ethoxy}benzene

Guidance literature:: Multi-step reaction with 4 steps

1: 74 percent / K₂CO₃ / dimethylformamide / 10 h / 80 °C

2: H₂ / 10percent Pd/C / methanol; CH₂Cl₂ / 5 h / 20 °C

3: 65 percent / K₂CO₃ / dimethylformamide / 168 h / 80 °C

4: 88 percent / Et₃N; DMAP / CH₂Cl₂ / 2 h / 20 °C

With dmap; hydrogen; potassium carbonate; triethylamine; 10percent Pd/C; In methanol; dichloromethane; N,N-dimethyl-formamide; 1: Alkylation / 2: Hydrogenolysis / 3: Alkylation / 4: Tosylation;
DOI:10.1002/(SICI)1099-0690(200002)2000:4<591::AID-EJOC591>3.0.CO;2-I

Reference yield:

: 264124-13-2
1-benzyloxy-4-[2-{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}ethoxy]benzene

: 264124-15-4
1-{2-[2-{2-[2-(4-methylphenylsulfonyloxy)ethoxy]ethoxy}ethoxy]ethoxy}-4-{2-[2-{2-[2-(4-triphenylmethylphenoxy)ethoxy]ethoxy}ethoxy]ethoxy}benzene

Guidance literature:: Multi-step reaction with 3 steps

1: H₂ / 10percent Pd/C / methanol; CH₂Cl₂ / 5 h / 20 °C

2: 65 percent / K₂CO₃ / dimethylformamide / 168 h / 80 °C

3: 88 percent / Et₃N; DMAP / CH₂Cl₂ / 2 h / 20 °C

With dmap; hydrogen; potassium carbonate; triethylamine; 10percent Pd/C; In methanol; dichloromethane; N,N-dimethyl-formamide; 1: Hydrogenolysis / 2: Alkylation / 3: Tosylation;
DOI:10.1002/(SICI)1099-0690(200002)2000:4<591::AID-EJOC591>3.0.CO;2-I