ChemicalBook--->CAS DataBase List--->648921-37-3

648921-37-3

648921-37-3 Structure

648921-37-3 Structure
IdentificationBack Directory
[Name]

3,3-DIMETHYL-PIPERIDIN-4-ONE HCL SALT
[CAS]

648921-37-3
[Synonyms]

3,3-DIMETHYL-PIPERIDIN-4-ONE HCL SALT
3,3-DiMethyl-4-piperidone Hydrochloride
4-Piperidinone, 3,3-dimethyl-, hydrochloride
3,3-Dimethyl-4-piperidinone hydrochloride (1:1)
[Molecular Formula]

C7H13NO.ClH
[MDL Number]

MFCD11043097
[MOL File]

648921-37-3.mol
[Molecular Weight]

163.647
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,Room Temperature
[Appearance]

Off-white to yellow Solid
Safety DataBack Directory
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

3,3-DIMETHYL-PIPERIDIN-4-ONE HCL SALT(648921-37-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-(tert-Butoxycarbonyl)-3,3-dimethyl-4-oxopiperidine

324769-06-4

3,3-DIMETHYL-PIPERIDIN-4-ONE HCL SALT

648921-37-3

General procedure for the synthesis of 3,3-dimethylpiperidin-4-one hydrochloride using 1-BOC-3,3-dimethyl-4-oxopiperidine as starting material: 1-BOC-3,3-dimethyl-4-oxopiperidine (2.0 g, 8.8 mmol) was dissolved in THF (30 mL) and concentrated hydrochloric acid (1.5 mL) was added slowly. The reaction mixture was stirred at room temperature and subsequently heated to 60 °C and maintained for 3 hours. Upon completion of the reaction, it was cooled to room temperature and white precipitate formation was observed. The precipitate was collected by filtration and dried to give 3,3-dimethylpiperidin-4-one hydrochloride (1.1 g, 78% yield). The product did not require further purification and could be used directly in the subsequent reaction.

[References]

[1] Patent: US2012/220629, 2012, A1. Location in patent: Page/Page column 45
[2] Patent: WO2012/113103, 2012, A1. Location in patent: Page/Page column 61
[3] Patent: WO2017/189386, 2017, A1. Location in patent: Page/Page column 44
[4] Patent: WO2018/136887, 2018, A1. Location in patent: Page/Page column 154
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