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3-Chlorobenzenesulphonyl chloride → Sodium 3-chlorobenzene-1-sulfinate

HRID 2036679
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2036679
S([O-])([O-])=O.[Na+:5].[Na+].C(=O)(O)[O-].[Na+].[Cl:12][C:13]1[CH:14]=[C:15]([S:19](Cl)(=[O:21])=[O:20])[CH:16]=[CH:17][CH:18]=1>O>[Cl:12][C:13]1[CH:14]=[C:15]([S:19]([O-:21])=[O:20])[CH:16]=[CH:17][CH:18]=1.[Na+:5]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 179093-Chlorobenzenesulphonyl chlorideHCID 24437Sodium SulfiteHCID 516892Sodium Bicarbonate

Produkt 1

HCID 23677431Sodium 3-chlorobenzene-1-sulfinateAusbeute 65,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

A solution of sodium sulphite (627 mg, 4.98 mmol) and sodium bicarbonate (418 mg, 4.98 mmol) in water (13 mL) was stirred vigorously with 3-chlorobenzenesulfonyl chloride (500 mg, 2.36 mmol) at 0° C. for 30 min then heated at 65° C. for 3 h. After cooling to ambient temperature, the reaction mixture was washed with dichloromethane (2×20 mL) and lyophilized. The resulting white solid was stirred with methanol (10 mL) for 5 min and the insoluble inorganic salts removed by filtration. The filtrate was concentrated in vacuo to approximately 3 mL and an equal volume of diethyl ether added. The precipitated solid containing residual inorganic salts was filtered and set aside. The remaining filtrate was diluted with excess diethyl ether, filtered and the filtered solid dried in vacuo to give sodium 3-chloro-benzenesulfinate (306 mg, 65%) as a white solid: 1H NMR (DMSO-d6, 300 MHz) δ 7.43 (br s, 1H), 7.35-7.39 (m, 1H), 7.32 (d, J=7.2 Hz, 1H), 7.26 (dt, J=7.5, 1.8 Hz, 1H).

Aufarbeitung

  1. temperatureAfter cooling to ambient temperature
  2. washthe reaction mixture was washed with dichloromethane (2×20 mL)
  3. customthe insoluble inorganic salts removed by filtration
  4. concentrationThe filtrate was concentrated in vacuo to approximately 3 mL
  5. additionan equal volume of diethyl ether added
  6. additionThe precipitated solid containing residual inorganic salts
  7. filtrationwas filtered
  8. additionThe remaining filtrate was diluted with excess diethyl ether
  9. filtrationfiltered
  10. customthe filtered solid dried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-b1aa2e7f437b488ab62b58392ec8abc6
Quelldatensatz
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08575186B2

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