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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Tributyl borate | HCID 12712 | — |
| Reactant | 2,4-Pentanedione, 3-benzyl- | HCID 97757 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Benzyl-1,7-diphenyl-1,6-heptadiene-3,5-dione | HCID 69501724 | 313.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841326B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-2e9fa605a42840959f88d791f2c4ede4 |
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| Source note | uspto-grants-2014_09 |
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