[(benzyloxycarbonyl)azanediyl]bis[(ethane-2,1-diyloxy)ethane-2,1-diyl] bis(4-methylbenzenesulfonate)

Base Information

Chemical Name:[(benzyloxycarbonyl)azanediyl]bis[(ethane-2,1-diyloxy)ethane-2,1-diyl] bis(4-methylbenzenesulfonate)
CAS No.:1315451-37-6
Molecular Formula:C₃₀H₃₇NO₁₀S₂
Molecular Weight:635.756
Hs Code.:

Synonyms:[(benzyloxycarbonyl)azanediyl]bis[(ethane-2,1-diyloxy)ethane-2,1-diyl] bis(4-methylbenzenesulfonate)

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Chemical Property of [(benzyloxycarbonyl)azanediyl]bis[(ethane-2,1-diyloxy)ethane-2,1-diyl] bis(4-methylbenzenesulfonate)

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Technology Process of [(benzyloxycarbonyl)azanediyl]bis[(ethane-2,1-diyloxy)ethane-2,1-diyl] bis(4-methylbenzenesulfonate)

There total 3 articles about [(benzyloxycarbonyl)azanediyl]bis[(ethane-2,1-diyloxy)ethane-2,1-diyl] bis(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: 67.0%

: 254448-30-1
2,2'-{[(benzyloxycarbonyl)azanediyl]bis(ethane-2,1-diyloxy)}diethanol

: 98-59-9
p-toluenesulfonyl chloride

: 1315451-37-6
[(benzyloxycarbonyl)azanediyl]bis[(ethane-2,1-diyloxy)ethane-2,1-diyl] bis(4-methylbenzenesulfonate)

Guidance literature:: With triethylamine; at 20 ℃; for 24h; Inert atmosphere;
DOI:10.1016/j.tet.2011.05.050

Reference yield:

: 54384-47-3
2,2'-((azanediylbis(ethane-2,1-diyl))bis(oxy))diethanol

: 1315451-37-6
[(benzyloxycarbonyl)azanediyl]bis[(ethane-2,1-diyloxy)ethane-2,1-diyl] bis(4-methylbenzenesulfonate)

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / water / 6 h / 20 °C

2: triethylamine / 24 h / 20 °C / Inert atmosphere

With sodium hydrogencarbonate; triethylamine; In water;
DOI:10.1016/j.tet.2011.05.050

Reference yield:

: 501-53-1,94274-21-2
benzyl chloroformate

: 1315451-37-6
[(benzyloxycarbonyl)azanediyl]bis[(ethane-2,1-diyloxy)ethane-2,1-diyl] bis(4-methylbenzenesulfonate)

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydrogencarbonate / water / 6 h / 20 °C

2: triethylamine / 24 h / 20 °C / Inert atmosphere

With sodium hydrogencarbonate; triethylamine; In water;
DOI:10.1016/j.tet.2011.05.050