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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77639Generated: October 24, 2026

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

https://huagongshe.com/en/reaction/77639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHydrochloric AcidHCID 313—
ReactantButylamineHCID 8007—
ReactantTributyl borateHCID 12712—
Reactant2,4-Pentanedione, 3-benzyl-HCID 97757—
SolventEthyl AcetateHCID 8857—
Product4-Benzyl-1,7-diphenyl-1,6-heptadiene-3,5-dioneHCID 69501724313.8%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841326B2
Source datasetuspto-grants-2014_09
ORD IDord-2e9fa605a42840959f88d791f2c4ede4
Source noteuspto-grants-2014_09