Hydrochloric Acid → HCID 57925897, compound
Reaction equation
C[O:2][C:3](=[O:19])[C:4]1[CH:9]=[CH:8][C:7]([C:10]([P:13]([O:17][CH3:18])([O:15][CH3:16])=[O:14])([F:12])[CH3:11])=[CH:6][CH:5]=1.[Li+].[OH-].Cl>O1CCOCC1>[CH3:16][O:15][P:13]([C:10]([C:7]1[CH:6]=[CH:5][C:4]([C:3]([OH:19])=[O:2])=[CH:9][CH:8]=1)([F:12])[CH3:11])([O:17][CH3:18])=[O:14]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
4-[1-(Dimethoxy-phosphoryl)-1-fluoro-ethyl]-benzoic acid methyl ester (0.56 g, 1.93 mmol) was made 0.25 M in dioxane and to this stirring solution was added 3 M aqueous LiOH (0.14 g, 5.79 mmol). The resulting mixture was stirred at ambient temperature for 18 hours. The mixture was neutralized with 1N aq HCl and concentrated in vacuo. The residue was carried forward without further purification: MS: cal'd 277 (MH+), exp 277 (MH+)
Workup
- concentrationconcentrated in vacuo
- customThe residue was carried forward without further purification
Sources & evidence
- ORD record
- ord-be3de6d22f5945ba8ef7184d49e5af94
- Source dataset
- uspto-grants-2011_07
- Patent number
- US07981874B2
Reaction notes
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