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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77635Erstellt: 23. Oktober 2026

Benzaldehyde → Dicinnamoylmethane

https://huagongshe.com/de/reaction/77635

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktHydrochloric AcidHCID 313—
EduktButylamineHCID 8007—
EduktTributyl borateHCID 12712—
EduktAcetylacetoneHCID 31261—
LösungsmittelEthyl AcetateHCID 8857—
ProduktDicinnamoylmethaneHCID 390472162,8%

Reaktionsschritte

Boric anhydride (0.49 g, 7.0 mmol) was combined with 2,4-pentanedione (2, 1.05 ml, 10.0 mmol) and stirred for 18 hr at room temperature under a nitrogen atmosphere. A solution of dry ethyl acetate (10 ml), benzaldehyde (1b, 2.05 g, 20.2 mmol) and tributyl borate (11.00 ml, 40.5 mmol) was added and the mixture stirred for 15 min at room temperature. Butylamine (0.20 ml, 2.0 mmol) was added dropwise over 30 min and stirring was continued for 18 hr at room temperature. Hydrochloric acid (15 ml, 0.4 N) was warmed to 60° C., added to the mixture and stirring was continued for 1 hr. The resulting mixture was extracted into ethyl acetate, washed with saturated sodium chloride, dried over magnesium sulfate, filtered and evaporated to afford a solid. The crude solid was triturated with methanol to give 0.90 g (33%) of a yellow solid: mp 140-142° C. [expected mp 139-140° C.]; 1H NMR: δ 5.84 (s, 1H), 6.62 (d, 2H, J=15.7 Hz), 7.39 (m, 6H), 7.54 (dd, 4H, J=7.4, 4.0 Hz), 7.66 (d, 2H, J=15.9 Hz), 15.85 (s, 1H); 13C NMR: δ 101.6, 124.1, 128.0, 128.9, 130.0, 135.0, 140.5, 183.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841326B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-998f773493e04693bd67be3f292a293a
Quellennotizuspto-grants-2014_09