Beta-Alanine → Pamidronic Acid
Reaction equation
P(Cl)(Cl)Cl.[NH2:5][CH2:6][CH2:7][C:8]([OH:10])=O.[P:11]([OH:14])([OH:13])[OH:12].C>O.ClC1C=CC=CC=1>[NH2:5][CH2:6][CH2:7][C:8]([OH:10])([P:11]([OH:14])(=[O:12])[OH:13])[P:11]([OH:14])(=[O:13])[OH:12]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
206 gm (1.5 mols) of phosphorus trichloride are slowly dropped while stirring into a mixture heated in a boiling water bath of 89.1 gm (1 mol) of β-alanine, 123 gm (1.5 mols) of phosphorous acid, and 500 ml of chlorobenzene, and heating on the boiling water bath is continued for a further 3 hours. During this time the contents of the flask become solid. After the reaction is finished, 600 ml of water are added and the product is heated for a short time, treated with animal charcoal and filtered while hot. The 3-amino-1-hydroxypropane-1,1-diphosphonic acid gradually crystallizes out from the aqueous phase in a cooling cabinet. The mother liquor is concentrated and treated with methanol, whereupon still further diphosphonic acid is precipitated. The 3-amino-1-hydroxypropane-1,1-diphosphonic acid is then recrystallized from water.
Workup
- temperaturethe product is heated for a short time
- filtrationfiltered while hot
- customThe 3-amino-1-hydroxypropane-1,1-diphosphonic acid gradually crystallizes out from the aqueous phase in a cooling cabinet
- concentrationThe mother liquor is concentrated
- additiontreated with methanol, whereupon still further diphosphonic acid
- customis precipitated
- customThe 3-amino-1-hydroxypropane-1,1-diphosphonic acid is then recrystallized from water
Sources & evidence
- ORD record
- ord-02c5b8fde724486f8447eff46f57d203
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04117086
Reaction notes
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