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N,N-Dimethylethylenediamine → HCID 13785476, Verbindung

HRID 1905771
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1905771
Cl[S:2]([C:5]1[CH:14]=[CH:13][CH:12]=[C:11]([N+:15]([O-:17])=[O:16])[C:6]=1[C:7]([O:9]C)=[O:8])(=[O:4])=[O:3].[CH3:18][N:19]([CH3:23])[CH2:20][CH2:21][NH2:22]>C1COCC1>[CH3:18][N:19]([CH3:23])[CH2:20][CH2:21][NH:22][S:2]([C:5]1[CH:14]=[CH:13][CH:12]=[C:11]([N+:15]([O-:17])=[O:16])[C:6]=1[C:7]([OH:9])=[O:8])(=[O:4])=[O:3]
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Komponenten

4

Edukt 2

HCID 66053N,N-DimethylethylenediamineHCID 13670189Methyl 2-(chlorosulfonyl)-6-nitrobenzoate

Produkt 1

HCID 13785476HCID 13785476, VerbindungAusbeute 16 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A solution of methyl 2-chlorosulfonyl-6-nitrobenzoate (500 mg, 1.79 mmol) and 2-dimethylaminoethylamine (316 mg, 3.58 mmol) in THF (35 ml) was stirred in an ice bath for 1 hour then at 20°-25° for 18 hours. After removing THF under reduced pressure, the residue was partitioned between saturated Na2CO3 solution and EtOAc. The organic extract was washed (saturated NaCl solution), dried (Na2SO4), filtered and concentrated under reduced pressure. Chromatography over silica gel (elution with 5% MeOH-95% CHCl3) gave an oil which when triturated with EtOAc afforded 2-[N-(2-dimethylaminoethyl)aminosulfonyl]-6-nitrobenzoic acid (90 mg, 16%), m.p. 193° decomposed with effervescence.

Aufarbeitung

  1. customAfter removing THF under reduced pressure
  2. customthe residue was partitioned between saturated Na2CO3 solution and EtOAc
  3. extractionThe organic extract
  4. washwas washed (saturated NaCl solution)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customChromatography over silica gel (elution with 5% MeOH-95% CHCl3) gave an oil which when
  9. customtriturated with EtOAc

Quellen und Nachweise

ORD-Eintrag
ord-31334d75a1fb43fdacd02ca7579916bc
Quelldatensatz
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04647588

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