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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395628Erstellt: 25. Oktober 2026

1,2,3,4-Tetrahydro-2-naphthalenol → 4-(4-Chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-[3-(5,6,7,8-tetrahydro-2-naphthoxy)propyl]oxazole

https://huagongshe.com/reaction/395628

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2,3,4-Tetrahydro-2-naphthalenolHCID 10747—
EduktTributylphosphineHCID 13831—
Edukt1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
Edukt4-(4-Chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanolHCID 9926997—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(4-Chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-[3-(5,6,7,8-tetrahydro-2-naphthoxy)propyl]oxazoleHCID 18174744—

Reaktionsschritte

To a mixture of 4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-oxazolepropanol (318 mg), 2-hydroxytetralin (296 mg), tributylphosphine (405 mg) and tetrahydrofuran (10 ml) was added 1,1′-(azodicarbonyl)dipiperidine (400 mg) at room temperature, and the resulting mixture was stirred for 1 hour. After the reaction mixture was concentrated, the residue was subjected to silica gel column chromatography, and 4-(4-chlorophenyl)-2-(2-methyl-1-imidazolyl)-5-[3-(5,6,7,8-tetrahydro-2-naphthoxy)propyl]oxazole was obtained as an oil from an ethyl acetate-hexane (1:1, v/v)-eluted fraction. (358 mg, 80%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605629B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-46c3a4ff77254cdb89118a2a89bc17fe
Quellennotizuspto-grants-2003_08