3-benzyl-2-n-capryl-1-(16-(2'-tetrahydropyranyloxy)hexadecyl)-rac-glycerol

Base Information

Chemical Name:3-benzyl-2-n-capryl-1-(16-(2'-tetrahydropyranyloxy)hexadecyl)-rac-glycerol
CAS No.:221637-71-4
Molecular Formula:C₃₉H₆₈O₆
Molecular Weight:632.965
Hs Code.:

Synonyms:3-benzyl-2-n-capryl-1-(16-(2'-tetrahydropyranyloxy)hexadecyl)-rac-glycerol

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Chemical Property of 3-benzyl-2-n-capryl-1-(16-(2'-tetrahydropyranyloxy)hexadecyl)-rac-glycerol

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Technology Process of 3-benzyl-2-n-capryl-1-(16-(2'-tetrahydropyranyloxy)hexadecyl)-rac-glycerol

There total 8 articles about 3-benzyl-2-n-capryl-1-(16-(2'-tetrahydropyranyloxy)hexadecyl)-rac-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: 100.0%

: 623-66-5
octanoic acid anhydride

: 221637-68-9
3-benzyl-1-(16-(2'-tetrahydropyranyloxy)hexadecyl)-rac-glycerol

: 221637-71-4
3-benzyl-2-n-capryl-1-(16-(2'-tetrahydropyranyloxy)hexadecyl)-rac-glycerol

Guidance literature:: With 4-pyrrolidin-1-ylpyridine; In chloroform; at 20 ℃;
DOI:10.1002/(SICI)1099-1344(199903)42:3<245::AID-JLCR184>3.0.CO;2-G

Reference yield:

: 110-87-2
3,4-dihydro-2H-pyran

: 221637-71-4
3-benzyl-2-n-capryl-1-(16-(2'-tetrahydropyranyloxy)hexadecyl)-rac-glycerol

Guidance literature:: Multi-step reaction with 4 steps

1: 33 percent / p-toluenesulfonic acid / tetrahydrofuran / 48 h / 0 - 20 °C

2: 45 percent / carbon tetrabromide; triphenylphosphine / benzene / 1 h / 20 °C

3: potassium t-butoxide; tetrabutylammonium bromide / benzene / 42 h / Heating

4: 100 percent / 4-pyrrolidinopyridine / CHCl₃ / 20 °C

With carbon tetrabromide; potassium tert-butylate; tetrabutylammomium bromide; 4-pyrrolidin-1-ylpyridine; toluene-4-sulfonic acid; triphenylphosphine; In tetrahydrofuran; chloroform; benzene; 1: Etherification / 2: Substitution / 3: Alkylation / 4: Acylation;
DOI:10.1002/(SICI)1099-1344(199903)42:3<245::AID-JLCR184>3.0.CO;2-G

Reference yield:

: 7735-42-4
1,16-hexadecanediol

: 221637-71-4
3-benzyl-2-n-capryl-1-(16-(2'-tetrahydropyranyloxy)hexadecyl)-rac-glycerol

Guidance literature:: Multi-step reaction with 4 steps

1: 33 percent / p-toluenesulfonic acid / tetrahydrofuran / 48 h / 0 - 20 °C

2: 45 percent / carbon tetrabromide; triphenylphosphine / benzene / 1 h / 20 °C

3: potassium t-butoxide; tetrabutylammonium bromide / benzene / 42 h / Heating

4: 100 percent / 4-pyrrolidinopyridine / CHCl₃ / 20 °C

With carbon tetrabromide; potassium tert-butylate; tetrabutylammomium bromide; 4-pyrrolidin-1-ylpyridine; toluene-4-sulfonic acid; triphenylphosphine; In tetrahydrofuran; chloroform; benzene; 1: Etherification / 2: Substitution / 3: Alkylation / 4: Acylation;
DOI:10.1002/(SICI)1099-1344(199903)42:3<245::AID-JLCR184>3.0.CO;2-G