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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1419064Erstellt: 26. Oktober 2026

Acetic Acid → alpha-(4-Benzyloxy-2-methoxyphenyl)-2-neopentylamino-5-chlorobenzyl alcohol

https://huagongshe.com/reaction/1419064

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktPivalaldehydeHCID 12417—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt2-Amino-alpha-(4-benzyloxy-2-methoxyphenyl)-5-chlorobenzyl alcoholHCID 53931958—
LösungsmittelEthanolHCID 702—
Produktalpha-(4-Benzyloxy-2-methoxyphenyl)-2-neopentylamino-5-chlorobenzyl alcoholHCID 54116645—

Reaktionsschritte

A mixture of 2-amino-α-(4-benzyloxy-2-methoxyphenyl)-5-chlorobenzyl alcohol (9.5 g), pivalaldehyde (3.35 ml), acetic acid (1.85 g) and ethanol (200 ml) was stirred for 30 min. To the mixture was added sodium cyanoborohydride (2.33 g) and the mixture was stirred for 24 h. After the mixture was concentrated in vacuo, the residue was diluted with water (200 ml) and extracted with ethyl acetate (200 ml). The extract was washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1) to give α-(4-benzyloxy-2-methoxyphenyl)-2-neopentylamino-5-chlorobenzyl alcohol (10.0 g) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05885979
Quelldatensatzuspto-grants-1999_03
ORD IDord-c51709c944854e20a4de4b585ef90007
Quellennotizuspto-grants-1999_03