ChemicalBook--->CAS DataBase List--->192436-83-2

192436-83-2

192436-83-2 Structure

192436-83-2 Structure
IdentificationBack Directory
[Name]

4-BROMO-N-METHOXY-N-METHYLBENZAMIDE
[CAS]

192436-83-2
[Synonyms]

4-BROMO-N-METHOXY-N-METHYLBENZAMIDE
Benzamide, 4-bromo-N-methoxy-N-methyl-
4-[Methoxy(methyl)carbamoyl]bromobenzene
[Molecular Formula]

C9H10BrNO2
[MDL Number]

MFCD02684303
[MOL File]

192436-83-2.mol
[Molecular Weight]

244.09
Chemical PropertiesBack Directory
[refractive index ]

1.5680 to 1.5720
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

clear liquid
[color ]

Colorless to Light yellow
[CAS DataBase Reference]

192436-83-2
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H315
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[HS Code ]

2928009090
Spectrum DetailBack Directory
[Spectrum Detail]

4-BROMO-N-METHOXY-N-METHYLBENZAMIDE(192436-83-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

N,O-Dimethylhydroxylamine hydrochloride

6638-79-5

4-Bromobenzoyl chloride

586-75-4

4-BROMO-N-METHOXY-N-METHYLBENZAMIDE

192436-83-2

To a stirred dichloromethane solution (300 mL) of 4-bromobenzoyl chloride (20.0 g, 91.1 mmol) was added triethylamine (28.0 mL, 200.0 mmol) and O,N-dimethylhydroxylamine hydrochloride (9.33 g, 95.6 mmol) at -78 °C. The reaction mixture was slowly warmed to room temperature and stirred continuously for 1.5 hours. After completion of the reaction, the mixture was concentrated to remove the solvent. The residue was ground with acetone and the solid obtained was dissolved in ethyl acetate and washed sequentially with water and brine. The organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated to give 4-bromo-N-methoxy-N-methylbenzamide (18.6 g, 84% yield).

[References]

[1] Angewandte Chemie - International Edition, 2010, vol. 49, # 17, p. 3073 - 3076
[2] Bioorganic and Medicinal Chemistry Letters, 2015, vol. 25, # 17, p. 3694 - 3698
[3] European Journal of Organic Chemistry, 2017, vol. 2017, # 46, p. 6840 - 6850
[4] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 4, p. 1415 - 1419
[5] Patent: US2007/66628, 2007, A1. Location in patent: Page/Page column 15
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