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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1885441Erstellt: 25. Oktober 2026

Acetate → Uniconazole

https://huagongshe.com/reaction/1885441

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetateHCID 175—
EduktAcetic AcidHCID 176—
EduktHydrochloric AcidHCID 313—
EduktSodium borohydrideHCID 4311764—
Edukt(E)-1-(4-chlorophenyl)-2-(1,2,4-triazol-1-yl)-4,4-dimethyl-1-penten-3-oneHCID 10913254—
Edukt(S)-(-)-2-Amino-4-methyl-1,1-diphenyl-1-pentanolHCID 10945486—
ProduktUniconazoleHCID 643660473%

Reaktionsschritte

Reaction was carried out in the same manner as in Example 1 except that the hydrochloride of (S)-2-amino-1,1-diphenyl-4-methylpentan-1-ol was replaced by the acetate thereof, the amount of sodium borohydride used was 0.075 g (1.98 mmoles), and that the reaction was carried out for 91 hours with addition of 0.0162 g (0.27 mmole) of acetic acid to (E)-1-(4-chlorophenyl)-2-(1,2,4-triazol-1-yl)-4,4-dimethyl-1-penten-3-one, to obtain (+)-(E)-1-(4-chlorophenyl)-2-(1,2,4-triazol-1-yl)-4,4-dimethyl-1-penten-3-ol. The conversion was 100%, and the composition of the product was: E-form alcohol, 90.3%; Z-form alcohol, 6.3%; and saturated alcohol, 3.4%. The enatiomer ratio of the E-form alcohol was: (+)-isomer, 86.5% and (-)-isomer, 13.5%. The optical yield was 73%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05144071
Quelldatensatzuspto-grants-1992_09
ORD IDord-ef98066fccea40289d620f137b95133e
Quellennotizuspto-grants-1992_09