Ethanol, 2-[2-(triphenylmethoxy)ethoxy]-, 1-(4-methylbenzenesulfonate)

Base Information

Chemical Name:Ethanol, 2-[2-(triphenylmethoxy)ethoxy]-, 1-(4-methylbenzenesulfonate)
CAS No.:141282-25-9
Molecular Formula:C30H30O5S
Molecular Weight:502.631
Hs Code.:
DSSTox Substance ID:DTXSID001154739
Mol file:141282-25-9.mol

Synonyms:141282-25-9;Ethanol, 2-[2-(triphenylmethoxy)ethoxy]-, 1-(4-methylbenzenesulfonate);2-(2-(Trityloxy)ethoxy)ethyl 4-methylbenzenesulfonate;SCHEMBL9523426;DTXSID001154739

Suppliers and Price of Ethanol, 2-[2-(triphenylmethoxy)ethoxy]-, 1-(4-methylbenzenesulfonate)

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of Ethanol, 2-[2-(triphenylmethoxy)ethoxy]-, 1-(4-methylbenzenesulfonate)

Chemical Property:

XLogP3:5.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:12
Exact Mass:502.18139523
Heavy Atom Count:36
Complexity:661

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)OCCOCCOC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4

Technology Process of Ethanol, 2-[2-(triphenylmethoxy)ethoxy]-, 1-(4-methylbenzenesulfonate)

There total 3 articles about Ethanol, 2-[2-(triphenylmethoxy)ethoxy]-, 1-(4-methylbenzenesulfonate) 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: 78.0%

: 105589-77-3
2-(2-trityloxyethoxy)ethanol

: 98-59-9
p-toluenesulfonyl chloride

: 141282-25-9
2-[2-(triphenylmethoxy)ethoxy]ethyl 4-methylbenzene-1-sulfonate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃;
DOI:10.1002/(SICI)1521-3765(20000317)6:6<1026::AID-CHEM1026>3.0.CO;2-C

Reference yield:

: 76-83-5
trityl chloride

: 141282-25-9
2-[2-(triphenylmethoxy)ethoxy]ethyl 4-methylbenzene-1-sulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / pyridine / 16 h / 40 °C

2: 78 percent / Et₃N / CH₂Cl₂ / 20 °C

With triethylamine; In pyridine; dichloromethane; 1: Etherification / 2: Tosylation;
DOI:10.1002/(SICI)1521-3765(20000317)6:6<1026::AID-CHEM1026>3.0.CO;2-C

Reference yield:

: 76-83-5
trityl chloride

: 141282-25-9
2-[2-(triphenylmethoxy)ethoxy]ethyl 4-methylbenzene-1-sulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: 57 percent / pyridine / 72 h / 20 °C

2: 51 percent / pyridine

With pyridine;