Hydrochloric Acid → HCID 13631101, compound
Reaction equation
[O:1]=[C:2]1[CH2:5][CH2:4][N:3]1[CH2:6][C:7]([O:9]CC)=[O:8].[OH-].[Na+].Cl>CO>[O:1]=[C:2]1[CH2:5][CH2:4][N:3]1[CH2:6][C:7]([OH:9])=[O:8]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
In 28 ml of methanol was dissolved 1.44 g of ethyl α-(2-oxo-1-azetidinyl)acetate (19) and 10 ml of a 1N sodium hydroxide aqueous solution was dropwise added to the solution under ice cooling. The mixture was reacted at 10° to 15° C. for 1 hour. The reaction solution was ice-cooled and 10 ml of 1N-hydrochloric acid was added thereto. Methanol was removed by distillation under reduced pressure. After the remaining aqueous solution was saturated with sodium chloride, the mixture was extracted 3 times with 140 ml of ethyl acetate. The ethyl acetate extracts were combined and dried over anhydrous sodium sulfate and then concentrated to obtain 950 mg of α-(2-oxo-1-azetidinyl)acetic acid (20).
Workup
- additionwas dropwise added to the solution under ice cooling
- customThe mixture was reacted at 10° to 15° C. for 1 hour
- temperaturecooled
- customMethanol was removed by distillation under reduced pressure
- extractionthe mixture was extracted 3 times with 140 ml of ethyl acetate
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-1a5cc4628cce4b1db21b8d41fddbde73
- Source dataset
- uspto-grants-1988_01
- Patent number
- US04719207
Reaction notes
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