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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77637Erstellt: 24. Oktober 2026

Benzaldehyde → 2,4-Pentanedione, 3-(phenylmethylene)-

https://huagongshe.com/de/reaction/77637

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktWaterHCID 962—
EduktAcetylacetoneHCID 31261—
KatalysatorAcetic AcidHCID 176—
KatalysatorPiperidineHCID 8082—
LösungsmittelBenzeneHCID 241—
Produkt2,4-Pentanedione, 3-(phenylmethylene)-HCID 9578295,3%

Reaktionsschritte

2,4-Pentanedione (2, 4.10 ml, 39.2 mmol) and benzaldehyde (1b, 4.06 ml, 40.0 mmol) were stirred in benzene (10 ml). Piperdine (3 drops) and glacial acetic acid (6 drops) were added and the mixture refluxed with a Dean-Stark water trap for 3 hr. The resulting mixture was cooled to room temperature, extracted into ethyl ether, washed with hydrochloric acid (1 N), saturated sodium bicarbonate, hydrochloric acid (1 N) and twice with water. The organic layer was dried over magnesium sulfate, filtered and evaporated to afford an oil. The crude oil was distilled bulb to bulb to give 7.03 g (95%) of a yellow oil; [expected mp 165-167° C.]; 1H NMR: δ 2.24 (s, 3H), 2.38 (s, 3H), 7.35 (s, 5H), 7.45 (s, 1H); 13C NMR: δ 26.5, 31.6, 128.9, 129.6, 130.5, 132.8, 139.6, 142.7, 196.2, 205.3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841326B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-8755114f947d4444af80e019f14ce045
Quellennotizuspto-grants-2014_09