Hydrochloric Acid → 89319-60-8
Reaction equation
[Na+].[C:2]([O:21][CH2:22][C@H:23]([CH2:44][O:45][P:46]([O:49][CH2:50][C@@H:51]([C:53]([O-:55])=[O:54])[NH2:52])([OH:48])=[O:47])[O:24]C(=O)CCCCCCC/C=C\CCCCCCCC)(=[O:20])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9]/[CH:10]=[CH:11]\[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19].C(O)C(N)(CO)CO.Cl.[Cl-].[K+].Cl>O>[C:2]([O:21][CH2:22][C@H:23]([CH2:44][O:45][P:46]([O:49][CH2:50][C@@H:51]([C:53]([OH:55])=[O:54])[NH2:52])([OH:48])=[O:47])[OH:24])(=[O:20])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9]/[CH:10]=[CH:11]\[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH3:19]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
After 1,2-dioleoyl-sn-glycero-3-phospho-L-serine sodium salt (SIGMA, P1060) (85 mg) was dissolved in distilled water (25 ml), 200 mM Tris-HCl buffer (pH 8.0) (1.5 ml) and 100 mM potassium chloride (1.5 ml) were added to the solution, and phospholipase A2 (0.3 ml) (10 mg/ml, 5 mM sodium acetate buffer (pH 5.0)) was further added thereto. The mixture was reacted at room temperature for 20 hours, and the pH was rendered 2 to 3 with 5M hydrochloric acid to terminate the reaction. After the reaction solution was concentrated to dryness, the residue was dissolved in a chloroform-methanol solvent mixture and the solution was adsorbed on silica gel column chromatography. Elution was performed with a chloroform-methanol solvent mixture to give 1-oleoyl-sn-glycero-3-phospho-L-serine.
Workup
- additionwas further added
- customThe mixture was reacted at room temperature for 20 hours
- customto terminate
- customthe reaction
- concentrationAfter the reaction solution was concentrated to dryness
- dissolutionthe residue was dissolved in a chloroform-methanol solvent mixture
- washElution
Sources & evidence
- ORD record
- ord-704ca18be92f42908d5ea0f2de32e3a5
- Source dataset
- uspto-grants-2007_04
- Patent number
- US07202040B2
Reaction notes
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