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1027345-07-8

1027345-07-8 Structure

1027345-07-8 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[HS Code ]

2904990090
Spectrum DetailBack Directory
[Spectrum Detail]

4-Fluoro-3-(trifluoromethylsulfonyl)benzenesulfonyl Chloride(1027345-07-8)1HNMR
4-Fluoro-3-(trifluoromethylsulfonyl)benzenesulfonyl Chloride(1027345-07-8)FT-IR
Hazard InformationBack Directory
[Synthesis]

1-FLUORO-2-[(TRIFLUOROMETHYL)SULFONYL]BENZENE

2358-41-0

4-Fluoro-3-(trifluoromethylsulfonyl)benzenesulfonyl Chloride

1027345-07-8

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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