HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266760Generated: October 26, 2026
(Diethoxyphosphinyl)acetic acid → 5-(4-Dimethylamino-phenyl)-penta-2,4-dienoic acid
https://huagongshe.com/reaction/2266760
Participants
| Role | Name | HCID | Charge |
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| Reactant | (Diethoxyphosphinyl)acetic acid | HCID 36704 | — |
| Reactant | 4-(Dimethylamino)-cinnamaldehyde | HCID 92224 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(4-Dimethylamino-phenyl)-penta-2,4-dienoic acid | HCID 71447235 | 62.9% |
Reaction Steps
Butyllithium (24 mL of 2.5 N solution) was added to 120 mL of anhydrous tetrahydrofuran (THF) at −65° C. A solution of diethylphosphonoacetic acid (5.5 g) in 45 mL of anhydrous THF was added dropwise to the stirred solution at −65° C. over a period of one hour. The resulting solution was stirred at −65° C. for an additional 30 minutes and then a solution of p-dimethylaminocinnamaldehyde (5.0 g) in 80 mL of anhydrous THF was added to the reaction at −65° C. over a period of 30 minutes. The reaction was stirred for one hour, allowed to warm to room temperature and then stirred overnight. The reaction was then quenched with 400 mL of water and extracted with 300 mL of ethyl acetate three times. The aqueous layer was acidified with 5% hydrochloric acid (11 mL) to a pH of 6.1. The solid formed was filtered, washed with 75 mL of water and dried to yield 3.83 g of the desired 5-(p-dimethylaminophenyl)-2,4-pentadienoic acid. 1H NMR (DMSO-d6, 300 MHz), δ(ppm) 7.34 (m, 3H), 6.82 (m, 2H), 6.70 (d, 2H), 5.84 (d, 1H), 2.94 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858664B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-99058a0d361c4530a9d1ca0780e8d547 |
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| Source note | uspto-grants-2010_12 |
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