| Identification | Back Directory | [Name]
4-Fluoro-3-(trifluoromethylsulfonyl)benzenesulfonyl Chloride | [CAS]
1027345-07-8 | [Synonyms]
EOS-62147 4-fluoro-3-(trifuoromethylsulfonyl)benzenesulfonyl chlo 4-Fluoro-3-(trifluoromethylsulfonyl)benzenesulfonyl Chloride 4-Fluoro-3-[(trifluoromethyl)sulphonyl]benzenesulphonyl chloride 4-fluoro-3-((trifluoroMethyl)sulfonyl)benzene-1-sulfonyl chloride Benzenesulfonyl chloride, 4-fluoro-3-[(trifluoromethyl)sulfonyl]- | [Molecular Formula]
C7H3ClF4O4S2 | [MDL Number]
MFCD16883063 | [MOL File]
1027345-07-8.mol | [Molecular Weight]
326.67 |
| Chemical Properties | Back Directory | [Boiling point ]
397.1±42.0 °C(Predicted) | [density ]
1.733±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [form ]
liquid | [color ]
Clear, pale amber/ lime |
| Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 3-(trifluoromethylsulfonyl)-4-fluorobenzenesulfonyl chloride from 1-fluoro-2-(trifluoromethanesulfonyl)benzene: 1-fluoro-2-(trifluoromethanesulfonyl)benzene (10.00 g, 43.83 mmol) was dissolved in chlorosulfuric acid (35.00 mL) and the reaction was heated for 5 hours at 120°C. After the reaction was completed, the mixture was slowly poured into a mixture consisting of crushed ice (100 g) and water (300 mL). The reaction mixture was extracted with dichloromethane (80 mL x 2) and the combined organic phases were washed with distilled water (200 mL x 2). The organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford 3-(trifluoromethylsulfonyl)-4-fluorobenzenesulfonyl chloride (12.60 g, 38.57 mmol, 88% yield), which could be used for the next reaction without further purification. Mass spectrum (ESI) m/z = 307 [M-Cl+OH-H]. 1H NMR (400 MHz, DMSO-d6): δ 8.25 (m, 1H), 8.15 (m, 1H), 7.73 (m, 1H). | [References]
[1] Patent: WO2017/101851, 2017, A1. Location in patent: Paragraph 0135; 0138 [2] Patent: WO2008/61208, 2008, A2. Location in patent: Page/Page column 30-31 [3] Synthesis, 2008, # 15, p. 2398 - 2404 [4] Journal of Medicinal Chemistry, 2008, vol. 51, # 21, p. 6902 - 6915 [5] Patent: US2009/318689, 2009, A1. Location in patent: Page/Page column 34 |
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NovoChemy Ltd.
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021-31261262/ 49 (0)17662837245 |
| Website: |
www.novochemy.com |
| Company Name: |
SynAsst Chemical.
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021-60343070 |
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www.chemicalbook.com/ShowSupplierProductsList15848/0_EN.htm |
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