HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Water → 5-Chloro-alpha-(2-chlorophenyl)-2-(2,4-dimethoxybenzyl)aminobenzyl alcohol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 2,4-Dimethoxybenzaldehyde | HCID 69175 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | (2-Amino-5-chlorophenyl)(2-chlorophenyl)methanol | HCID 11437092 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 5-Chloro-alpha-(2-chlorophenyl)-2-(2,4-dimethoxybenzyl)aminobenzyl alcohol | HCID 53841495 | 96,1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05726306 |
| Quelldatensatz | uspto-grants-1998_03 |
| ORD ID | ord-8208d819f879448fbecf7d2aa5f1ad04 |
| Quellennotiz | uspto-grants-1998_03 |