(3-O-[2-(4-isobutylphenyl propanoyl)]-(S)-2-O-palmitoylglyceryl)-2-bromoethyl-methyl phosphate

Base Information

Chemical Name:(3-O-[2-(4-isobutylphenyl propanoyl)]-(S)-2-O-palmitoylglyceryl)-2-bromoethyl-methyl phosphate
CAS No.:322468-41-7
Molecular Formula:C₃₅H₆₀BrO₈P
Molecular Weight:719.734
Hs Code.:

Synonyms:(3-O-[2-(4-isobutylphenyl propanoyl)]-(S)-2-O-palmitoylglyceryl)-2-bromoethyl-methyl phosphate

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Chemical Property of (3-O-[2-(4-isobutylphenyl propanoyl)]-(S)-2-O-palmitoylglyceryl)-2-bromoethyl-methyl phosphate

Chemical Property:

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Technology Process of (3-O-[2-(4-isobutylphenyl propanoyl)]-(S)-2-O-palmitoylglyceryl)-2-bromoethyl-methyl phosphate

There total 4 articles about (3-O-[2-(4-isobutylphenyl propanoyl)]-(S)-2-O-palmitoylglyceryl)-2-bromoethyl-methyl 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:

: 322468-27-9
((S)-2-O-benzyl-glyceryl)-2-bromoethyl-methylphosphate

: 322468-41-7
(3-O-[2-(4-isobutylphenyl propanoyl)]-(S)-2-O-palmitoylglyceryl)-2-bromoethyl-methyl phosphate

Guidance literature:: Multi-step reaction with 3 steps

1: DCC; DMAP / CH₂Cl₂ / 2 h

2: H₂ / 10 percent Pd/C / CH₂Cl₂ / 2 h / 787.56 Torr

3: DCC; DMAP / CH₂Cl₂ / 2 h

With dmap; hydrogen; dicyclohexyl-carbodiimide; palladium on activated charcoal; In dichloromethane;
DOI:10.1016/S0009-3084(00)00167-5

Reference yield:

: phosphorous acid 2-benzyloxy-3-(tert-butyl-diphenyl-silanyloxy)-propyl ester 2-bromo-ethyl ester methyl ester

: 322468-41-7
(3-O-[2-(4-isobutylphenyl propanoyl)]-(S)-2-O-palmitoylglyceryl)-2-bromoethyl-methyl phosphate

Guidance literature:: Multi-step reaction with 5 steps

1: 30 percent aq.H₂O₂ / CH₂Cl₂ / 2 h

2: 90 percent / TBAF / tetrahydrofuran / 1 h

3: DCC; DMAP / CH₂Cl₂ / 2 h

4: H₂ / 10 percent Pd/C / CH₂Cl₂ / 2 h / 787.56 Torr

5: DCC; DMAP / CH₂Cl₂ / 2 h

With dmap; tetrabutyl ammonium fluoride; hydrogen; dihydrogen peroxide; dicyclohexyl-carbodiimide; palladium on activated charcoal; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0009-3084(00)00167-5

Reference yield:

: 322468-31-5
(3-O-[2-(4-isobutlyphenyl propanoyl)]-(S)-2-O-benzylglyceryl)-2-bromoethyl-methyl phosphate

: 322468-41-7
(3-O-[2-(4-isobutylphenyl propanoyl)]-(S)-2-O-palmitoylglyceryl)-2-bromoethyl-methyl phosphate

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / 10 percent Pd/C / CH₂Cl₂ / 2 h / 787.56 Torr

2: DCC; DMAP / CH₂Cl₂ / 2 h

With dmap; hydrogen; dicyclohexyl-carbodiimide; palladium on activated charcoal; In dichloromethane;
DOI:10.1016/S0009-3084(00)00167-5