Hydrochloric Acid → N-(2-methoxy-4-nitrophenyl)methanesulfonamide

HRID 19971

Reaktionsgleichung

Reaktionsgleichung von HRID 19971
[CH3:1][O:2][C:3]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[CH:7]=[CH:6][C:4]=1[NH2:5].[CH3:13][S:14](Cl)(=[O:16])=[O:15].Cl>N1C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:9]=[C:8]([N+:10]([O-:12])=[O:11])[CH:7]=[CH:6][C:4]=1[NH:5][S:14]([CH3:13])(=[O:16])=[O:15]

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 73372-Methoxy-4-nitroanilineHCID 31297Methanesulfonyl chloride

Produkt 1

HCID 3298129N-(2-methoxy-4-nitrophenyl)methanesulfonamideAusbeute 98 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1049PyridineLösungsmittel

Versuchsvorschrift

To a solution of 2-methoxy-4-nitroaniline (5 g) in pyridine (25 ml) at 0° C. was added dropwise methanesulfonyl chloride (3.5 ml). The mixture was left at 0° C. for 1 hour, then brought to RT for 2 h. The mixture was poured onto ice (100 g) and dilute hydrochloric acid (3M, 100 ml), the solid formed was filtered then washed with water and dried to give 2-methoxy-4-nitro-methanesulfonylaminobenzene (7.32 g, 98%) as an off-white crystalline solid.

Aufarbeitung

  1. waitbrought to RT for 2 h
  2. customthe solid formed
  3. filtrationwas filtered
  4. washthen washed with water
  5. customdried

Quellen und Nachweise

ORD-Eintrag
ord-6d014a8243e04485a2b10f8b84a064aa
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07745490B2

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