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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21524Erstellt: 25. Oktober 2026

Diazald → 1-Diazo-3-{o-[5-(2,4-dichlorophenoxy)-2-nitrophenoxy]phenoxy}-2-propanone

https://huagongshe.com/reaction/21524

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiazaldHCID 6628—
EduktPotassium HydroxideHCID 14797—
EduktHCID 19932413HCID 19932413—
LösungsmittelMethanolHCID 887—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Diazo-3-{o-[5-(2,4-dichlorophenoxy)-2-nitrophenoxy]phenoxy}-2-propanoneHCID 54022969—

Reaktionsbedingungen

Temperatur42 °C

Reaktionsschritte

A mixture of potassium hydroxide in methanol (20.0 mL of a 4M solution ) is heated to 42° C. and treated dropwise with a mixture of N-methyl-N-nitroso-p-toluenesulfonamide (4 g, 18.7 mmol) in ether (40 mL). The diazomethane is distilled over, condensed with a dry ice/acetone condenser and collected. The diazomethane/ether solution is stirred in an ice-bath, treated dropwise with a solution of {o-[5-(2,4-dichlorophenoxy)-2-nitrophenoxy]phenoxy}acetyl chloride (1.09 g, 2.32 mmol) in tetrahydrofuran, stirred for 30 minutes and concentrated in vacuo to give the title product as a yellow oil which is identified by NMR spectral analyses.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05424280
Quelldatensatzuspto-grants-1995_06
ORD IDord-d1f6cb8854ac44ce91cca18716b94224
Quellennotizuspto-grants-1995_06