Hydrochloric Acid → HCID 57925887, compound
Reaction equation
C([O:5][C:6]([C:8]1[CH:13]=[CH:12][C:11](CP(=O)O)=[CH:10][CH:9]=1)=[O:7])(C)(C)C.[CH2:18]([O:20][P:21]([C:24]1[CH:36]=[CH:35][C:27](C(OC(C)(C)C)=O)=[CH:26][CH:25]=1)(C)=[O:22])C.[OH-].[K+].Cl>O1CCOCC1>[CH3:18][O:20][P:21]([C:11]1[CH:10]=[CH:9][C:8]([C:6]([OH:5])=[O:7])=[CH:13][CH:12]=1)([C:24]1[CH:36]=[CH:35][CH:27]=[CH:26][CH:25]=1)=[O:22]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
[4-(tert-Butoxycarbonyl)phenyl]methylphosphinic acid]. tert-Butyl 4-[ethoxy(methyl) phosphoryl]benzoate (510 mg, 1.79 mmol) was made 0.25 M in dioxane and to this stirring solution was added potassium hydroxide (5.38 mL, 5.38 mmol). The resulting mixture was stirred at ambient temperature for 10 minutes. The reaction mixture was neutralized with 1 eq aq HCl then concentrated in vacuo. The residue was diluted with MeOH, the inorganic salts were filtered off and the filtrate was concentrated in vacuo. MS: cal'd 257 (MH+), exp 257 (MH+).
Workup
- concentrationthen concentrated in vacuo
- additionThe residue was diluted with MeOH
- filtrationthe inorganic salts were filtered off
- concentrationthe filtrate was concentrated in vacuo
Sources & evidence
- ORD record
- ord-818630fb9f374a8fb6b59293ea09848c
- Source dataset
- uspto-grants-2011_07
- Patent number
- US07981874B2
Reaction notes
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