ChemicalBook--->CAS DataBase List--->40724-47-8

40724-47-8

40724-47-8 Structure

40724-47-8 Structure
IdentificationBack Directory
[Name]

4-BROMOMETHYL-BENZENESULFONAMIDE
[CAS]

40724-47-8
[Synonyms]

4-sulfonamide benzyl bromide
p-Bromomethylbenzenesulfonamide
4-BROMOMETHYL-BENZENESULFONAMIDE
Benzenesulfonamide, 4-(bromomethyl)-
4-(broMoMethyl)benzene-1-sulfonaMide
[Molecular Formula]

C7H8BrNO2S
[MDL Number]

MFCD08752696
[MOL File]

40724-47-8.mol
[Molecular Weight]

250.11
Chemical PropertiesBack Directory
[Melting point ]

191-192℃
[Boiling point ]

386.4±44.0 °C(Predicted)
[density ]

1.691
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

9.99±0.10(Predicted)
[Appearance]

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


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362
Spectrum DetailBack Directory
[Spectrum Detail]

4-BROMOMETHYL-BENZENESULFONAMIDE(40724-47-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

alpha-Bromo-p-toluenesulphonyl chloride

66176-39-4

4-BROMOMETHYL-BENZENESULFONAMIDE

40724-47-8

General procedure for the synthesis of p-bromomethylbenzenesulfonamide from 4-bromomethylbenzenesulfonyl chloride: 4.1 Synthesis of acetylsulfonamide (SZ2TA1): ammonia was passed into a solution of compound 1 (1 g, 3.7 mmol) in dichloromethane (DCM, 100 mL) at 0°C for 10 min. Subsequently, brine (20 mL) was added for quenching. The organic phase was separated, dried over anhydrous sodium sulfate, and concentrated. Purification by fast chromatography (eluent ratio: hexane:EtOAc = 2:1) afforded product 17 (900 mg, 96.8% yield). 1H-NMR (250 MHz, acetone-d6) δ: 7.91 (d, J = 10.0 Hz, 2H), 7.67 (d, J = 10.0 Hz, 2H), 6.63 (bs, 2H), 4.74 (s, 2H) ppm.

[References]

[1] ChemMedChem, 2011, vol. 6, # 5, p. 816 - 825
[2] Journal of the American Chemical Society, 2008, vol. 130, # 42, p. 13820 - 13821
[3] Patent: WO2012/21486, 2012, A2. Location in patent: Page/Page column 113; 114
[4] Patent: WO2012/21486, 2012, A2. Location in patent: Page/Page column 96; 97
[5] ACS Medicinal Chemistry Letters, 2018, vol. 9, # 5, p. 462 - 467
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