Sodium Hydroxide → Silver(1+) dibenzyl phosphate
Reaction equation
[P:1]([O-:19])([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:2].[OH-].[Na+].[N+]([O-])([O-])=O.[Ag+:26]>O>[P:1]([O-:19])([O:3][CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:2].[Ag+:26]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Dibenzyl phosphate (2.78 g, 10 mmol) in water (40 mL) was cooled in an ice bath. Subsequently, 1N NaOH was added while shaking the flask until the pH of solution was about 7. The solid dissolved almost completely. Then silver nitrate (1.89 g, 11 mmol) in water (20 mL) was added slowly. After adding, the resulting solid was collected by filtration and washed with water. The solid was dried in vacuum over phosphorus pentoxide to yield silver dibenzyl phosphate (3.18 g) (yield, 82.5%) as a white solid.
Workup
- dissolutionThe solid dissolved almost completely
- additionAfter adding
- filtrationthe resulting solid was collected by filtration
- washwashed with water
- dry with materialThe solid was dried in vacuum over phosphorus pentoxide
Sources & evidence
- ORD record
- ord-3a37b49b2b3f4dc0b9fe1b0ad6857f72
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09079928B2
Reaction notes
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