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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 714154Erstellt: 24. Oktober 2026

Benzaldehyde → 4-Benzyl-1,7-diphenyl-1,6-heptadiene-3,5-dione

https://huagongshe.com/de/reaction/714154

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktHydrochloric AcidHCID 313—
EduktButylamineHCID 8007—
EduktTributyl borateHCID 12712—
Edukt2,4-Pentanedione, 3-benzyl-HCID 97757—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-Benzyl-1,7-diphenyl-1,6-heptadiene-3,5-dioneHCID 69501724313,8%

Reaktionsschritte

Boric anhydride (0.49 g, 7.0 mmol) was combined with 3-benzyl-2,4-pentanedione (8, 1.90 g, 10.0 mmol) and stirred for 48 hr at room temperature under a nitrogen atmosphere. A solution of dry ethyl acetate (10 ml), benzaldehyde (1b, 2.05 ml, 20.2 mmol) and tributyl borate (11.0 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 filtered to afford a solid. The crude solid was triturated with methanol to give 2.30 g (63%) of a yellow solid: mp 162-164° C. [expected mp 156-158° C.]; 1H NMR: δ 3.99 (s, 2H), 6.99 (d, 2H, J=15.6 Hz), 7.34 (m, 15H), 7.77 (d, 2H, J=15.2 Hz); 13C NMR: δ 31.8, 109.3, 120.8, 126.5, 127.8, 128.1, 128.8, 130.0, 135.3, 140.5, 141.9, 183.6.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09187397B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-5c9d7cb901ef403d94e6dc554e231ee0
Quellennotizuspto-grants-2015_11