3-O-[26-Benzyloxy-3,6,9,12,15,18,21,24-octaoxahexacosyl]-1,2-di-O-hexadecyl-sn-glycerol

Base Information

Chemical Name:3-O-[26-Benzyloxy-3,6,9,12,15,18,21,24-octaoxahexacosyl]-1,2-di-O-hexadecyl-sn-glycerol
CAS No.:260351-13-1
Molecular Formula:C₆₀H₁₁₄O₁₂
Molecular Weight:1027.56
Hs Code.:

Synonyms:3-O-[26-Benzyloxy-3,6,9,12,15,18,21,24-octaoxahexacosyl]-1,2-di-O-hexadecyl-sn-glycerol

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Chemical Property of 3-O-[26-Benzyloxy-3,6,9,12,15,18,21,24-octaoxahexacosyl]-1,2-di-O-hexadecyl-sn-glycerol

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Technology Process of 3-O-[26-Benzyloxy-3,6,9,12,15,18,21,24-octaoxahexacosyl]-1,2-di-O-hexadecyl-sn-glycerol

There total 9 articles about 3-O-[26-Benzyloxy-3,6,9,12,15,18,21,24-octaoxahexacosyl]-1,2-di-O-hexadecyl-sn-glycerol 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: 89.0%

: 105891-50-7
1-chloro-10-phenyl-3,6,9-trioxadecane

: 260351-12-0
1,2-Di-O-hexadecyl-3-O-[17-hydroxy-3,6,9,12,15-pentaoxaheptadecyl]-sn-glycerol

: 260351-13-1
3-O-[26-Benzyloxy-3,6,9,12,15,18,21,24-octaoxahexacosyl]-1,2-di-O-hexadecyl-sn-glycerol

Guidance literature:: With tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran; Heating;
DOI:10.1002/(SICI)1521-3765(20000103)6:1<111::AID-CHEM111>3.0.CO;2-X

Reference yield:

: 5197-62-6
2-[2-(chloroethoxy)ethoxy]ethanol

: 260351-13-1
3-O-[26-Benzyloxy-3,6,9,12,15,18,21,24-octaoxahexacosyl]-1,2-di-O-hexadecyl-sn-glycerol

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / NaH / dimethylformamide / 20 °C

2: 89 percent / NaH; tetrabutylammonium iodide / tetrahydrofuran / Heating

3: 99 percent / H₂ / 10 percent Pd/C / tetrahydrofuran / 16 h

4: 89 percent / NaH; tetrabutylammonium iodide / tetrahydrofuran / Heating

With hydrogen; tetra-(n-butyl)ammonium iodide; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; N,N-dimethyl-formamide; 1: Etherification / 2: Etherification / 3: Hydrogenolysis / 4: Etherification;
DOI:10.1002/(SICI)1521-3765(20000103)6:1<111::AID-CHEM111>3.0.CO;2-X

Reference yield:

: 105891-50-7
1-chloro-10-phenyl-3,6,9-trioxadecane

: 260351-13-1
3-O-[26-Benzyloxy-3,6,9,12,15,18,21,24-octaoxahexacosyl]-1,2-di-O-hexadecyl-sn-glycerol

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / NaH; tetrabutylammonium iodide / tetrahydrofuran / Heating

2: 99 percent / H₂ / 10 percent Pd/C / tetrahydrofuran / 16 h

3: 89 percent / NaH; tetrabutylammonium iodide / tetrahydrofuran / Heating

With hydrogen; tetra-(n-butyl)ammonium iodide; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; 1: Etherification / 2: Hydrogenolysis / 3: Etherification;
DOI:10.1002/(SICI)1521-3765(20000103)6:1<111::AID-CHEM111>3.0.CO;2-X