ChemicalBook--->CAS DataBase List--->130596-62-2

130596-62-2

130596-62-2 Structure

130596-62-2 Structure
IdentificationBack Directory
[Name]

4,4-dimethyl-1,4-azasilinane hydrochloride
[CAS]

130596-62-2
[Synonyms]

4,4-DIMETHYL-1,4-AZASILINANE HCL
4,4-dimethyl-1,4-azasilinane hydrochloride
4,4-dimethyl-4-silapiperidine hydrochloride
1-Aza-4-silacyclohexane, 4,4-dimethyl-, hydrochloride (1:1)
[Molecular Formula]

C6H16ClNSi
[MDL Number]

MFCD28399395
[MOL File]

130596-62-2.mol
[Molecular Weight]

165.74
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,2-8°C
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C6H15NSi.ClH/c1-8(2)5-3-7-4-6-8;/h7H,3-6H2,1-2H3;1H
[InChIKey]

GAKCLWKKNFVTPB-UHFFFAOYSA-N
[SMILES]

C[Si]1(CCNCC1)C.Cl
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H319-H302-H315
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P
Spectrum DetailBack Directory
[Spectrum Detail]

4,4-dimethyl-1,4-azasilinane hydrochloride(130596-62-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-Aza-4-silacyclohexane, 4,4-dimethyl-1-(phenylmethyl)-

130596-60-0

4,4-dimethyl-1,4-azasilinane hydrochloride

130596-62-2

General procedure for the synthesis of 4,4-dimethyl-1,4-azasilane hydrochloride from the compound (CAS:130596-60-0): 6N HCl (10.5 mmol) was added to an ethanol (EtOH) solution of compound 3 (2.3 g, 10.5 mmol), followed by removal of solvent under reduced pressure. The reaction mixture was co-evaporated with EtOH (2 x 10 mL) and recrystallized from a mixed EtOH-ether solvent. The ethanol solution of the resulting HCl salt was added dropwise to the slurry of Pd/C in EtOH, and the reaction was stirred for 20 h at 25 °C under hydrogen atmosphere. Upon completion of the reaction, the mixture was filtered through diatomaceous earth and the filter cake was washed with methanol (2 x 20 mL). The filtrate was concentrated under reduced pressure to give a viscous oil, which was subsequently titrated with ether to give the final product 4 as a white solid (950 mg) in 70% yield. The synthesis of this compound was previously documented in patent WO 2006/066872.

[References]

[1] Patent: WO2013/54275, 2013, A1. Location in patent: Page/Page column 18-19; 22
[2] Patent: US2014/296133, 2014, A1. Location in patent: Paragraph 0075; 0092
[3] ACS Medicinal Chemistry Letters, 2015, vol. 6, # 11, p. 1105 - 1110
[4] Patent: CN107266421, 2017, A. Location in patent: Paragraph 0094; 0095; 0096
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