Identification | Back Directory | [Name]
N-(2-broMophenyl)-N-Methyl-MethanesulfonaMide | [CAS]
553652-34-9 | [Synonyms]
Silanecarboxamide,N,N,1,1,3-pentamethyl- N-(2-broMophenyl)-N-Methyl-MethanesulfonaMide Methanesulfonamide, N-(2-bromophenyl)-N-methyl- | [Molecular Formula]
C8H10BrNO2S | [MDL Number]
MFCD25542385 | [MOL File]
553652-34-9.mol | [Molecular Weight]
264.14 |
Chemical Properties | Back Directory | [Boiling point ]
333.6±44.0 °C(Predicted) | [density ]
1.604±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Store in freezer, under -20°C | [pka]
-3.03±0.50(Predicted) | [Appearance]
White to off-white Solid |
Hazard Information | Back Directory | [Synthesis]
GENERAL STEPS: To a suspension of N-(2-bromophenyl)methane sulfonamide (5.01 g, 20.0 mmol) and cesium carbonate (7.2 g, 22 mmol) in acetonitrile (20 mL) was added iodomethane (1.4 mL, 22 mmol). The reaction mixture was stirred at room temperature for 24 hours. Upon completion of the reaction, the reaction mixture was diluted with dichloromethane (30 mL), filtered through a diatomaceous earth plug and the filtrate was concentrated under reduced pressure. N-(2-bromophenyl)-N-methylmethanesulfonamide was obtained as a light orange solid (5.22 g, 98% yield). The product was characterized by 1H NMR (400 MHz, CDCl3, δ, ppm): 7.65 (d, J = 8.0 Hz, 1H), 7.50 (d, J = 7.9 Hz, 1H), 7.37 (t, J = 7.4 Hz, 1H), 7.23 (t, J = 8.2 Hz, 1H), 3.29 (s, 3H), 3.06 (s, 3H). Mass spectrometry (MS) analysis showed m/z = 286,288 (MH+). | [References]
[1] Patent: WO2010/141796, 2010, A2. Location in patent: Page/Page column 276 [2] Patent: EP3287463, 2018, A1. Location in patent: Paragraph 0104; 0110 [3] Tetrahedron, 2014, vol. 70, # 49, p. 9359 - 9365 [4] Patent: US2018/208604, 2018, A1. Location in patent: Paragraph 0372-0373 |
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Company Name: |
BePharm Ltd
|
Tel: |
400-685-9117 |
Website: |
www.bepharm.com |
Company Name: |
Energy Chemical
|
Tel: |
021-58432009 400-005-6266 |
Website: |
http://www.energy-chemical.com |
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