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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1941471Erstellt: 26. Oktober 2026

N-Benzyl-N-nitroso-p-toluenesulfonamide → Benzene, (diazomethyl)-

https://huagongshe.com/reaction/1941471

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-Benzyl-N-nitroso-p-toluenesulfonamideHCID 4118076—
EduktSodium MethoxideHCID 10942334—
LösungsmittelMethanolHCID 887—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
ProduktBenzene, (diazomethyl)-HCID 13660130%

Reaktionsschritte

N-Nitroso-N-benzyl-p-toluene sulphonamide (966 mg, 3.33 mmol) was added in small portions to a solution of sodium methoxide (2.0 ml of 2M solution in methanol) in t-butyl methyl ether (12 ml) and methanol (2 ml) at room temperature. After the addition was finished the reaction mixture was refluxed for 15-30 min. The reaction mixture was cooled and washed with water (3×6 ml). The ethereal solution of phenyl diazomethane was dried over sodium sulphate for 30 minutes. The solvent was removed in vacuo and the residue distilled under reduce pressure to give phenyl diazomethane as a dark red oil (30% yield, b.p. 20° C. at 1 mmHg) which was immediately dissolved in t-butyl methyl ether (6 ml).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05703246
Quelldatensatzuspto-grants-1997_12
ORD IDord-f49d6f158adc41dfba6332ceeb0af4e9
Quellennotizuspto-grants-1997_12