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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967064Generated: October 30, 2026

Phosphorus oxychloride → 3-Methyl-5-phenyl-2,4-pentadienoic acid

https://huagongshe.com/reaction/1967064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant3-Methyl-1-phenyl-buten-3-olHCID 92677—
ReactantSodium AcetateHCID 517045—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-Methyl-5-phenyl-2,4-pentadienoic acidHCID 77493863.4%

Reaction Steps

Dimethylformamide (DMF, anhydrous, 25 mL) was cooled to 0-5° C. and phosphorus oxychloride (16.4 mL) was added dropwise over a period of an hour. The resulting solution was added dropwise to a cooled (0-5° C.) solution of 4-phenyl-2-methyl-3-buten-2-ol (0.14 mol) in 60 mL of anhydrous DMF over a period of an hour. The reaction mixture was then warmed to room temperature, gradually heated up to 80° C., stirred at 80° C. for three hours and cooled to 0-5° C. To the cooled reaction solution was added dropwise a solution of sodium acetate (80 g) in deionized water (190 mL) over a period of two hours. The mixture was then reheated to 80° C., stirred at 80° C. for an additional 10 minutes, cooled down to room temperature and extracted with ether (300 mL) twice. The combined extract was washed with water (200 mL), dried over anhydrous sodium sulfate, filtered and concentrated in vacuum to yield 16.7 g of the desired 3-methyl-5-phenyl-2,4-pentadienal as a liquid which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420698B2
Source datasetuspto-grants-2013_04
ORD IDord-1c20cf95659b4ebb849787fbb46c0dde
Source noteuspto-grants-2013_04