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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 235788Erstellt: 27. Oktober 2026

Benzaldehyde → 3-amino-5-benzylaminobenzoic Acid

https://huagongshe.com/reaction/235788

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
Edukt3,5-Diaminobenzoic acidHCID 12062—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelMethanolHCID 887—
Produkt3-amino-5-benzylaminobenzoic AcidHCID 20217441—

Reaktionsschritte

15.2 g. (0.1 mol) of 3,5-diaminobenzoic acid was placed in a 500 ml. round bottom flask to which 200 ml of methanol was added. To the round bottom flask 10.3 g. (0.1 mol) of benzaldehyde was added. The solution was stirred for several minutes. While the solution stirred 3.77 g. (0.06 mol) sodium cyanoborohydride was added slowly. After 5 hours the solution was filtered and then concentrated to dryness. The reaction mixture was dissolved in 200 ml. of 2M hydrochloric acid. The acid solution was extracted twice with 200 ml. ethyl acetate. The ethyl acetate solutions were combined and back washed with 200 ml. distilled water, and then dried over sodium sulfate. The solution was concentrated to dryness and 4.58 gm. of product was collected. The product was then purified by column chromatography using a solution of tetrahydrofuran/ethanol/water/ammonium hydroxide in the following ratio--10:3:1:0.04 as the eluent. Structural verification was obtained by carbon magnetic resonance, proton magnetic resonance and infra-red analysis.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04642240
Quelldatensatzuspto-grants-1987_02
ORD IDord-ef3e66d1683c4992a20e6d24a63fea4c
Quellennotizuspto-grants-1987_02