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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77636Generated: October 25, 2026

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

https://huagongshe.com/reaction/77636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantButylamineHCID 8007—
ReactantTributyl borateHCID 12712—
Reactant3-Methyl-2,4-pentanedioneHCID 69949—
SolventEthyl AcetateHCID 8857—
Product4-Methyl-1,7-diphenyl-1,6-heptadiene-3,5-dioneHCID 69501726310%

Reaction Steps

Boric anhydride (0.49 g, 7.0 mmol) was combined with 3-methyl-2,4-pentanedione (5, 1.14 g, 10.0 mmol) and stirred for 24 hr at room temperature under a nitrogen atmosphere. A solution of 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 24 hr at room temperature. The resulting mixture was filtered to afford a solid. The crude solid was triturated with methanol to give 1.80 g (62%) of an orange solid: mp 154-157° C. [expected mp 154-157° C.]; 1H NMR: δ 2.17 (s, 3H), 7.12 (d, 2H, J=15.5 Hz), 7.38 (m, 6H), 7.58 (m, 4H), 7.74 (d, 2H, J=15.5 Hz); 13C NMR: δ 12.1, 106.2, 120.8, 182.1, 128.8, 129.9, 135.4, 141.3, 182.4. Anal. Calcd for C20H18O2: C, 82.73; H, 6.25. Found: C, 82.69; H, 6.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841326B2
Source datasetuspto-grants-2014_09
ORD IDord-3d438f05a2d9468c92e3939d32888650
Source noteuspto-grants-2014_09