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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2259185Erstellt: 26. Oktober 2026

Water → N-(1,1-Dimethylethyl)-2-[(methoxyimino)methyl]-1H-pyrrole-3-sulfonamide

https://huagongshe.com/reaction/2259185

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium AcetateHCID 517045—
EduktO-Methylhydroxylamine hydrochlorideHCID 521874—
EduktN-(1,1-Dimethylethyl)-2-formyl-1-methyl-1H-pyrrole-3-sulfonamideHCID 19693840—
LösungsmittelMethanolHCID 887—
ProduktN-(1,1-Dimethylethyl)-2-[(methoxyimino)methyl]-1H-pyrrole-3-sulfonamideHCID 13614480696,2%

Reaktionsschritte

To a suspension of 3.91 g (46.8 mmol) of methoxyamine hydrochloride in 60 mL of methanol was added 3.84 g (46.8 mmol) of sodium acetate. After stirring the white suspension for ca. 15 minutes 5.72 g (23 mmol) of N-(1,1-dimethylethyl)-2-formyl-1-methyl-1H-pyrrole-3-sulfonamide was added in one portion. The white suspension was heated at a gentle reflux overnight ca. 16 hours. The reaction mixture was cooled to room temperature and poured into 500 mL of water. The aqueous mixture was extracted with four 100 mL portions of methylene chloride. The combined extracts were washed with water, dried (MgSO4) and concentrated in vacuo yielding 5.74 g of the title compound as a white solid, m.p. 99°-101° C. 1H NMR (CDCl3, 200 MHz.) δ: 8.51(s,1H), 6.66(d,1H), 6.54(d,1H), 4.82(bs,1H), 3.97(s,3H), 3.82(s,3H), 1.24(s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05472933
Quelldatensatzuspto-grants-1995_12
ORD IDord-9fd3c49acc3949dbaeffb920eeba00e0
Quellennotizuspto-grants-1995_12