Nitric Acid → Mono nitro-benzo[b]thiophene-2-sulfonyl chloride

HRID 244288

Reaktionsgleichung

Reaktionsgleichung von HRID 244288
[S:1]1[C:5]([S:6]([Cl:9])(=[O:8])=[O:7])=[CH:4][C:3]2[CH:10]=[CH:11][CH:12]=[CH:13][C:2]1=2.[N+:14]([O-])([OH:16])=[O:15]>ClCCl>[N+:14]([C:4]1[C:3]2[CH:10]=[CH:11][CH:12]=[CH:13][C:2]=2[S:1][C:5]=1[S:6]([Cl:9])(=[O:8])=[O:7])([O-:16])=[O:15]

Komponenten

4

Edukt 2

HCID 944Nitric AcidHCID 27763331-Benzothiophene-2-sulfonyl chloride

Produkt 1

HCID 15158699Mono nitro-benzo[b]thiophene-2-sulfonyl chloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a solution of benzo[b]thiophene-2-sulfonyl chloride (1.165 g, 5 mmol) in 25 mL of dichloromethane was added 3.6 mL of concentrated nitric acid (>22.05 mol/L) dropwise, the resulting mixture was refluxed overnight and cooled to room temperature before it was poured into 20 gram of crushed ice. The organic layer was separated and the aqueous layer was extracted by 220 mL 2 dichloromethane. The organic layers were combined and dried over MgSO4. Solvent was then removed by rotary evaporator. The crude product was purified by flash column chromatography with an eluent of hexane, followed by a gradient eluent of hexane/ethyl acetate (6/1-3/1) to afford 0.58 g of product (mixture of 65% of 4-nitro-benzo[b]thiophene-2-sulfonyl chloride and 35% of 7-nitro-benzo[b]thiophene-2-sulfonyl chloride).

Aufarbeitung

  1. temperaturethe resulting mixture was refluxed overnight
  2. customThe organic layer was separated
  3. extractionthe aqueous layer was extracted by 220 mL 2 dichloromethane
  4. dry with materialdried over MgSO4
  5. customSolvent was then removed by rotary evaporator
  6. customThe crude product was purified by flash column chromatography with an eluent of hexane

Quellen und Nachweise

ORD-Eintrag
ord-5c6c5bae08bf4cc09943f99760e11f27
Quelldatensatz
uspto-grants-2014_02
Patentnummer
US08658345B2

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