Trifluoromethane sulfonic acid-[1,3-bis-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-prop-2-yl]-ester

Base Information

Chemical Name:Trifluoromethane sulfonic acid-[1,3-bis-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-prop-2-yl]-ester
CAS No.:872462-83-4
Molecular Formula:C₃₈H₄₃F₃O₉S
Molecular Weight:732.815
Hs Code.:

Synonyms:Trifluoromethane sulfonic acid-[1,3-bis-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-prop-2-yl]-ester

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

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Chemical Property of Trifluoromethane sulfonic acid-[1,3-bis-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-prop-2-yl]-ester

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Technology Process of Trifluoromethane sulfonic acid-[1,3-bis-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-prop-2-yl]-ester

There total 1 articles about Trifluoromethane sulfonic acid-[1,3-bis-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-prop-2-yl]-ester 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: 82.0%

: 358-23-6
trifluoromethylsulfonic anhydride

: 138208-14-7
1,9-di-O-benzyl-2,8-bis(benzyloxymethyl)-3,7-dioxanonane

: 872462-83-4
Trifluoromethane sulfonic acid-[1,3-bis-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-prop-2-yl]-ester

Guidance literature:: With 2,6-dimethylpyridine; In dichloromethane; at -20 ℃; for 2h;

Reference yield: 71.0%

: 872462-83-4
Trifluoromethane sulfonic acid-[1,3-bis-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-prop-2-yl]-ester

: 156536-14-0
2-amino-1,3-bis(1,3-dibenzyl-2-glyceroxy)-2-propane

Guidance literature:: Trifluoromethane sulfonic acid-[1,3-bis-(2-benzyloxy-1-benzyloxymethyl-ethoxy)-prop-2-yl]-ester; With sodium azide; In N,N-dimethyl acetamide; water; at 60 ℃; for 12h;

With lithium aluminium tetrahydride; In diethyl ether; at 20 ℃; for 4h;