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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 714155Erstellt: 24. Oktober 2026

Water → 4,4-Dibenzyl-1,7-diphenyl-1,6-heptadiene-3,5-dione

https://huagongshe.com/de/reaction/714155

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktBenzyl BromideHCID 7498—
EduktSodium HydroxideHCID 14798—
EduktDicinnamoylmethaneHCID 390472—
KatalysatorTetrabutylammonium ChlorideHCID 70681—
LösungsmittelDichloromethaneHCID 6344—
Produkt4,4-Dibenzyl-1,7-diphenyl-1,6-heptadiene-3,5-dioneHCID 69501774121,7%

Reaktionsschritte

1,7-Diphenyl-1,6-heptadiene-3,5-dione (3b, 0.25 g, 0.9 mmol) was stirred in dichloromethane (4 ml) for 5 min at room temperature. A solution of sodium hydroxide (80.0 mg, 2.0 mmol), tetrabutylammonium chloride (0.29 g, 1.0 mmol) and water (2 ml) was added and the mixture stirred for 10 min at room temperature. Benzyl bromide (10, 0.22 ml, 1.8 mmol) was added and the mixture stirred for 1 hr at 40° C. The resulting mixture was cooled to room temperature, washed with saturated sodium chloride, dried over magnesium sulfate, filtered and evaporated to afford a solid. The crude solid was chromatographed on silica gel with ethyl acetate/hexane to give a solid. The solid was recrystallized from methanol to give 0.25 g (61%) of a white solid: mp 182-183° C. [expected mp 181° C.]; 1H NMR: δ 3.39 (s, 4H), 6.70 (d, 2H, J=15.5 Hz), 7.09-7.44 (m, 20H), 7.73 (d, 2H, J=15.5 Hz); 13C NMR: δ 37.7, 70.3, 123.1, 126.7, 128.1, 128.6, 128.8, 130.3, 130.7, 134.2, 136.3, 142.7, 196.8.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09187397B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-c64a444d3f1f4c898cdab58c7e7ba27b
Quellennotizuspto-grants-2015_11