Sulfuric Acid → HCID 21556755, Verbindung

HRID 267290Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 267290
S(=O)(=O)(O)O.[Br:6][C:7]1[C:12]([CH:13]([CH2:15][CH3:16])[CH3:14])=[CH:11][C:10]([S:17](Cl)(=O)=O)=[C:9]([CH:21]([CH2:23][CH3:24])[CH3:22])[CH:8]=1>[Zn]>[Br:6][C:7]1[C:12]([CH:13]([CH2:15][CH3:16])[CH3:14])=[CH:11][C:10]([SH:17])=[C:9]([CH:21]([CH2:23][CH3:24])[CH3:22])[CH:8]=1

Komponenten

4

Versuchsvorschrift

A 128-ml portion of concentrated sulfuric acid was added to 300 g of ice while keeping the temperature at 0°-10°C. Then 41 g of 4-bromo-2,5-di-sec-butylbenzenesulfonyl chloride was added. While maintaining the temperature at 0°-10°C, 65 g of zinc dust was added with good agitation over a period of 2 hours. The reaction mixture was then heated under reflux on a steam bath for 5 hours. After cooling, the mixture was extracted into methylene dichloride, dried over magnesium sulfate, filtered, and concentrated to an oil which was distilled, to give 27 g of 4-bromo-2,5-di-sec-butylbenzenethiol, bp 106°-107°C/0.22 mm, nD25 1.5599.

Aufarbeitung

  1. customat 0°-10°C
  2. temperatureWhile maintaining the temperature at 0°-10°C
  3. temperatureThe reaction mixture was then heated
  4. temperatureunder reflux on a steam bath for 5 hours
  5. temperatureAfter cooling
  6. extractionthe mixture was extracted into methylene dichloride
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated to an oil which
  10. distillationwas distilled

Quellen und Nachweise

ORD-Eintrag
ord-1ebf4483d0454bc588225bf5b6e85b63
Quelldatensatz
uspto-grants-1976_03
Patentnummer
US03941826

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