ChemicalBook--->CAS DataBase List--->218772-96-4

218772-96-4

218772-96-4 Structure

218772-96-4 Structure
IdentificationBack Directory
[Name]

(4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE
[CAS]

218772-96-4
[Synonyms]

4-piperidon-1-acetic acid
1-Piperidineacetic acid, 4-oxo-
2-(4-Oxo-1-piperidyl)acetic Acid
2-(4-Oxopiperidin-1-yl)acetic acid
2-(4-oxo-1-piperidinyl)acetic acid hydrochloride
(4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE
[Molecular Formula]

C7H11NO3
[MDL Number]

MFCD07371475
[MOL File]

218772-96-4.mol
[Molecular Weight]

157.17
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
Safety DataBack Directory
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Synthesis]

tert-Butyl bromoacetate

5292-43-3

4,4-Piperidinediol hydrochloride

40064-34-4

(4-OXO-PIPERIDIN-1-YL)-ACETIC ACID HYDROCHLORIDE

218772-96-4

Step 1. 4-Piperidone monohydrate hydrochloride (5 g, 0.033 mol) was mixed with tert-butyl bromoacetate (6.98 g, 0.037 mol) and potassium carbonate (13.65 g, 0.099 mol) in dimethylformamide (100 ml) and reacted for 24 hours at 100 °C. After completion of the reaction, the mixture was cooled and concentrated in vacuum. The residue was partitioned between saturated potassium carbonate solution and ether (2 x 50 ml). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and evaporated to dryness to give 7.36 g of tert-butyl 2-(4-oxopiperidin-1-yl)acetate in 94% yield. The product was characterized by 1H NMR (CDCl3): δ 1.45 (9H, s), 2.45 (4H, t, J=7Hz), 2.3-2.4 (4H, m), 3.29 (2H, s).

[References]

[1] Patent: US6281226, 2001, B1
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