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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22868Erstellt: 24. Oktober 2026

Formic Acid → Formamide, N-(4-bromophenyl)-

https://huagongshe.com/de/reaction/22868

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormic AcidHCID 284—
Edukt4-BromoanilineHCID 7807—
EduktAcetic AnhydrideHCID 7918—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktFormamide, N-(4-bromophenyl)-HCID 1747499,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A 5-Liter round bottom flask was charged with acetic anhydride (488 mL, 5.2 mol) and cooled to 0° C. Formic acid (240 mL, 6.4 mol) was then added at a rate that did not elevate the temperature of the reaction mixture above 10° C. After the formic acid was added, the temperature of the reaction was raised to 50-60° C. and stirred for 3 hours. The reaction was then cooled to 0° C. and 400 mL of THF was added. A solution of 4-bromoaniline (344 g, 2.0 mol) in 800 mL of THF was added dropwise. After the addition was complete, the reaction was allowed to stir at this temperature for 4 hours. The reaction was checked by thin-layer chromatography and found to be complete. The reaction mixture was transferred to a round bottom flask and the solvent was removed in vacuo. When the solvent had been removed, the residue crystallized. The solid was triturated with heptane and filtered. Obtained 396.8 grams of desired N-(4-bromo-phenyl)-formamide. Yield 99.2% The spectral properties of the solid were consistent with the desired material. Step (2): (4-bromo-phenyl)-methyl-amine

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06849648B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-46bb61989247402b83f957372f1f9da2
Quellennotizuspto-grants-2005_02