ChemicalBook--->CAS DataBase List--->1193389-40-0

1193389-40-0

1193389-40-0 Structure

1193389-40-0 Structure
IdentificationBack Directory
[Name]

1-(4-BROMOPHENYL)CYCLOBUTANAMINE (HYDROCHLORIDE)
[CAS]

1193389-40-0
[Synonyms]

KML-40
CML-039
1-(4-broMophenyl)cyclobutanaMine
1-(4-Bromophenyl)-cyclobutanamine HCl
1-(4-BROMOPHENYL)CYCLOBUTANAMINE (HYDROCHLORIDE)
1-(4-broMophenyl)cyclobutan-1-aMine hydrochloride
Cyclobutanamine, 1-(4-bromophenyl)-, hydrochloride (1:1)
[Molecular Formula]

C10H13BrClN
[MDL Number]

MFCD09864775
[MOL File]

1193389-40-0.mol
[Molecular Weight]

262.574
Chemical PropertiesBack Directory
[storage temp. ]

Inert atmosphere,Room Temperature
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H319-H315-H335
[Precautionary statements ]

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

1-(4-BROMOPHENYL)CYCLOBUTANAMINE (HYDROCHLORIDE)(1193389-40-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-(4-bromophenyl)cyclobutane-1-carboxamide

1032350-05-2

1-(4-BROMOPHENYL)CYCLOBUTANAMINE (HYDROCHLORIDE)

1193389-40-0

Step 2: 1-(4-Bromophenyl)cyclobutane-1-carboxamide (8.120 g, 31.952 mmol) was dissolved in 1-butanol (50 mL), and sodium hypochlorite (11.00% aqueous, 25.101 mL, 44.733 mmol) and sodium hydroxide (3.00 M aqueous, 29.822 mL, 89.466 mmol) were added in sequence . The reaction mixture was stirred at room temperature for 18 hours. After completion of the reaction, the mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The concentrate was redissolved in ethyl acetate, hydrochloric acid (4.00 M solution of 1,4-dioxane, 11.982 mL, 47.928 mmol) was added and stirred. The precipitated solid was filtered, washed with ethyl acetate and dried to give 1-(4-bromophenyl)cyclobutanamine hydrochloride (3.320 g, 39.6% yield) as a white solid.

[References]

[1] Patent: KR2017/43091, 2017, A. Location in patent: Paragraph 1332; 1339-11341
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