triethylammonium 1,2-di-O-benzyl-sn-glyceryl 1-sn-glyceryl phosphate

Base Information

Chemical Name:triethylammonium 1,2-di-O-benzyl-sn-glyceryl 1-sn-glyceryl phosphate
CAS No.:1360874-33-4
Molecular Formula:C₆H₁₅N*C₂₀H₂₇O₈P
Molecular Weight:527.595
Hs Code.:

Synonyms:triethylammonium 1,2-di-O-benzyl-sn-glyceryl 1-sn-glyceryl phosphate

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Chemical Property of triethylammonium 1,2-di-O-benzyl-sn-glyceryl 1-sn-glyceryl phosphate

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Technology Process of triethylammonium 1,2-di-O-benzyl-sn-glyceryl 1-sn-glyceryl phosphate

There total 4 articles about triethylammonium 1,2-di-O-benzyl-sn-glyceryl 1-sn-glyceryl phosphate 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: 96.0%

: 1360874-31-2
triethylammonium 1,2-di-O-benzyl-sn-glyceryl 2,3-O-isopropylidene-sn-glycerylphosphate

: 1360874-33-4
triethylammonium 1,2-di-O-benzyl-sn-glyceryl 1-sn-glyceryl phosphate

Guidance literature:: With trifluoroacetic acid; at 20 ℃; for 0.0166667h;
DOI:10.1002/anie.201106470

Reference yield:

: 141263-13-0
triethylammonium 1,2-di-O-benzyl-sn-glyceryl hydrogenphosphonate

: 1360874-33-4
triethylammonium 1,2-di-O-benzyl-sn-glyceryl 1-sn-glyceryl phosphate

Guidance literature:: Multi-step reaction with 2 steps

1.1: pyridine; pivaloyl chloride / tetrahydrofuran / 0.03 h / 0 - 20 °C

1.2: 0.5 h / 20 °C

2.1: trifluoroacetic acid / 0.02 h / 20 °C

With pyridine; pivaloyl chloride; trifluoroacetic acid; In tetrahydrofuran;
DOI:10.1002/anie.201106470

Reference yield:

: 58530-76-0
(R)-2,3-dibenzyloxy-1-propanol

: 1360874-33-4
triethylammonium 1,2-di-O-benzyl-sn-glyceryl 1-sn-glyceryl phosphate

Guidance literature:: Multi-step reaction with 3 steps

1.1: pyridine; diphenyl phosphite / 1.17 h / 0 - 20 °C

1.2: 1 h / 20 °C

2.1: pyridine; pivaloyl chloride / tetrahydrofuran / 0.03 h / 0 - 20 °C

2.2: 0.5 h / 20 °C

3.1: trifluoroacetic acid / 0.02 h / 20 °C

With pyridine; diphenyl phosphite; pivaloyl chloride; trifluoroacetic acid; In tetrahydrofuran;
DOI:10.1002/anie.201106470