3-BROMO-4-METHOXY-BENZENESULFONYL CHLORIDE
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
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
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
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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