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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1772Erstellt: 23. Oktober 2026

Water → 5-Chloro-alpha-(2-chlorophenyl)-2-(2,4-dimethoxybenzyl)aminobenzyl alcohol

https://huagongshe.com/de/reaction/1772

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt2,4-DimethoxybenzaldehydeHCID 69175—
EduktSodium borohydrideHCID 4311764—
Edukt(2-Amino-5-chlorophenyl)(2-chlorophenyl)methanolHCID 11437092—
LösungsmittelAcetic AcidHCID 176—
Produkt5-Chloro-alpha-(2-chlorophenyl)-2-(2,4-dimethoxybenzyl)aminobenzyl alcoholHCID 5384149596,1%

Reaktionsschritte

To a solution of 2-amino-5-chloro-α-(2-chloro phenyl)benzyl alcohol (5.0 g) and 2,4-dimethoxy benzaldehyde (3.72 g) in acetic acid (50 ml) was added, under ice-cooling, sodium borohydride (0.94 g). The mixture was stirred for one hour at room temperature, which was poured into water (200 ml), followed by extraction with ethyl acetate (200 ml×2). The ethyl acetate layer was washed with 1N sodium hydroxide, which was dried over anhydrous magnesium sulfate, followed by distilling off the solvent under reduced pressure. The residue was purified by means of a silica gel column chromatography (hexane:ethyl acetate=5:1) to give 5-chloro-α-(2-chlorophenyl)-2-(2,4-dimethoxybenzyl)aminobenzyl alcohol (7.5 g) as an oily product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726306
Quelldatensatzuspto-grants-1998_03
ORD IDord-8208d819f879448fbecf7d2aa5f1ad04
Quellennotizuspto-grants-1998_03