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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714151Generated: October 27, 2026

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

https://huagongshe.com/reaction/714151

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 numberUS09187397B2
Source datasetuspto-grants-2015_11
ORD IDord-a3c8df7fc79a45f987c39c4fec0a70ac
Source noteuspto-grants-2015_11