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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11222Erstellt: 23. Oktober 2026

Cyclopropanecarboxaldehyde → 4-((3,5-Bis(trifluoromethyl)benzyloxy)methyl)-1-(cyclopropylmethyl)-4-phenylazepane

https://huagongshe.com/de/reaction/11222

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclopropanecarboxaldehydeHCID 123114—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt4-((3,5-Bis(trifluoromethyl)benzyloxy)methyl)-4-phenylazepaneHCID 11626160—
KatalysatorTrifluoroacetic acidHCID 6422—
LösungsmittelMethanolHCID 887—
Produkt4-((3,5-Bis(trifluoromethyl)benzyloxy)methyl)-1-(cyclopropylmethyl)-4-phenylazepaneHCID 2197311841,5%

Reaktionsschritte

Mixture of isomer A of 4-((3,5-bis(trifluoromethyl)benzyloxy)methyl)-4-phenylazepane (3 mg) and cyclopropanecarbaldehyde (1.4 mg) in methanol (0.15 mL) was stirred at room temperature for 0.5 hr, then sodium cyanoborohydride (1.0 M solution in THF, 0.02 mL) was added followed by 1 drop of trifluoroacetic acid. The mixture was stirred at room temperature for overnight and concentrated under vacuum. Then saturated sodium bicarbonate and dichloromethane was added to the mixture and the organic layer was separated. The aqueous layer was extracted with dichloromethane 2 times and the combined organic layers were dried over magnesium sulfate, filtered and concentrated under vacuum to give the product as a clear sticky oil (1.4 mg, 41% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07098203B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-55ba5bde656147629274f122dc38c215
Quellennotizuspto-grants-2006_08