Basic information Safety Supplier Related

3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE

Basic information Safety Supplier Related

3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE Basic information

Product Name:
3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE
Synonyms:
  • 3-bromo-4-methoxybenzenesulfonyl chloride(SALTDATA: FREE)
  • 3-broMo-4-Methoxybenzene-1-sulfonyl chloride
  • 3-Bromo-4-methoxybenzenesulfonyl chloride 97%
  • Benzenesulfonyl chloride, 3-bromo-4-methoxy-
  • 3-Bromo-4-methoxybenzenesulfonylchloride,97%
CAS:
23094-96-4
MF:
C7H6BrClO3S
MW:
285.54
Mol File:
23094-96-4.mol
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3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE Chemical Properties

Melting point:
83-88°C
Boiling point:
366.0±27.0 °C(Predicted)
Density 
1.717±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
Appearance
Off-white to pink Solid
Sensitive 
Moisture Sensitive
CAS DataBase Reference
23094-96-4
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Safety Information

Hazard Codes 
C
Risk Statements 
22-34
Safety Statements 
26-36/37/39-45
RIDADR 
UN 3261 8 / PGII
WGK Germany 
3
HazardClass 
IRRITANT
HazardClass 
8
HS Code 
2930909899
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3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE Usage And Synthesis

Synthesis

578-57-4

23094-96-4

General procedure for the synthesis of 3-bromo-4-methoxybenzene-1-sulfonyl chloride from 2-bromoanisole: 2-bromo-1-methoxybenzene (1.87 g, 10.0 mmol) was dissolved in chloroform (5 mL), and the solution was cooled in an iced salt bath to -5 °C to 0 °C. Chlorosulfonic acid (2.0 mL, 30.0 mmol) was slowly added dropwise over 30 minutes, and after completion of the dropwise addition, the reaction mixture was gradually warmed to room temperature over 1 hour. Subsequently, the reaction mixture was poured onto crushed ice and transferred to a dispensing funnel. The aqueous layer was separated and extracted twice with chloroform. The organic layers were combined, dried and concentrated to give 3-bromo-4-methoxybenzenesulfonyl chloride (2.80 g, 98%). 3-Bromo-4-methoxybenzenesulfonyl chloride (2.80 g, 9.8 mmol) was dissolved in dichloromethane (30 mL), triethylamine (1.76 mL, 12.6 mmol) was added to the solution, followed by slow dropwise addition of tert-butylamine (1.33 mL, 12.6 mmol). The reaction mixture was allowed to stand for 2 hours and then poured into a mixture of 5% citric acid solution and dichloromethane. The organic layer was separated and the aqueous layer was extracted twice with dichloromethane. The organic layers were combined, dried and concentrated. The crude product was recrystallized by ethyl acetate/hexane mixed solvent to give 3-bromo-N-tert-butyl-4-methoxybenzenesulfonamide (2.43 g, 77%).

References

[1] Patent: WO2004/50637, 2004, A2. Location in patent: Page 68-69
[2] Patent: WO2004/62661, 2004, A1. Location in patent: Page/Page column 24-25; 37-38
[3] Patent: US2015/25068, 2015, A1. Location in patent: Paragraph 0794
[4] Journal of the Chemical Society [Section] C: Organic, 1969, p. 1341 - 1345
[5] Bioorganic and Medicinal Chemistry Letters, 1997, vol. 7, # 4, p. 485 - 488

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