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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2085230Erstellt: 26. Oktober 2026

Salicylaldehyde → alpha-(2'-Hydroxybenzylidene)-delta-valerolactone

https://huagongshe.com/reaction/2085230

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSalicylaldehydeHCID 6998—
EduktDelta-ValerolactoneHCID 10953—
LösungsmittelTolueneHCID 1140—
Produktalpha-(2'-Hydroxybenzylidene)-delta-valerolactoneHCID 6970438227,5%

Reaktionsschritte

Salicylaldehyde (15.2 g) and δ-valerolactone (25 g) were dissolved in toluene (150 ml). By the reaction in the same manner as in Example 307, oily α-(2′-hydroxybenzylidene)-δ-valerolactone (7.0 g) was obtained. Dimethylformamide (70 ml) and potassium carbonate (9.5 g) were added hereto and (S) -glycidyl nosylate (8.9 g) was added. The mixture was stirred at 40° C. for 2 hr. The reaction mixture was concentrated under reduced pressure. Water was added and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the oily title compound (7.8 g). The reaction in the same manner as in Example 307 using this product (1.0 g) and 4-(naphthalen-2-yl)piperidine (1.0 g) in methanol (50 ml) was performed and the obtained oil was recrystallized from ethyl acetate to give the title compound (0.38 g), melting point 142-144° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06720320B2
Quelldatensatzuspto-grants-2004_04
ORD IDord-7f35f8d2bbe74c748a47e2ed8866d6c6
Quellennotizuspto-grants-2004_04