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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299592Generated: October 25, 2026

(Diethoxyphosphinyl)acetic acid → 5-(4-Dimethylamino-phenyl)-penta-2,4-dienoic acid

https://huagongshe.com/reaction/2299592

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethoxyphosphinyl)acetic acidHCID 36704—
Reactant4-(Dimethylamino)-cinnamaldehydeHCID 92224—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product5-(4-Dimethylamino-phenyl)-penta-2,4-dienoic acidHCID 7144723562.9%

Reaction Conditions

Temperature-65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495719B2
Source datasetuspto-grants-2002_12
ORD IDord-e434ec8f71374f94bbe275f7ac7946a4
Source noteuspto-grants-2002_12