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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929573Generated: October 27, 2026

2-(4-Fluorophenyl)acetic acid → 4-(4-Fluoro-phenyl)-2-methyl-buta-2,3-dienoic acid ethyl ester

https://huagongshe.com/reaction/1929573

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Fluorophenyl)acetic acidHCID 9837—
ReactantOxalyl chlorideHCID 65578—
ReactantEthyl 2-(triphenylphosphoranylidene)propionateHCID 79792—
ReactantDiisopropylethylamineHCID 81531—
SolventDimethylformamideHCID 6228—
SolventHeptaneHCID 8900—
Solventtert-Butyl methyl etherHCID 15413—
Product4-(4-Fluoro-phenyl)-2-methyl-buta-2,3-dienoic acid ethyl esterHCID 11481404—

Reaction Steps

To a solution of (4-fluoro-phenyl)-acetic acid (22.33 g, 144.9 mmol) in 100 mL of methyl tert-butyl ether and 250 μL of DMF was added 13.02 mL (146.3 mmol) of oxalyl chloride at room temperature dropwise over 30 minutes. The resulting mixture was stirred at room temperature for an additional 20 minutes (HPLC indicated completed reaction), and then the entire solution was added dropwise over 1 hour to a solution of N,N-diisopropylethylamine (50.48 mL, 289.8 mmol) and ethyl 2-(triphenylphosphoranylidene)propionate (50.0 g, 138.0 mmol) in 100 mL of methyl tert-butyl ether, while maintaining the internal temperature between 0-15° C. After the addition was complete, the reaction mixture was stirred for an additional 10 minutes at 0-10° C., when HPLC indicated a completed reaction. The reaction mixture was then diluted with 100 mL of heptane, and stirred for 30 minutes at 0-10° C. The resulting solid was filtered and washed with 2×100 mL of 1:1 methyl tert-butyl ether:heptane. The filtrate and the washings were combined and washed with 100 mL of water, 100 mL of 1M citric acid, 2×100 mL of water, then concentrated azeotropically at 25° C./60 mmHg to a total volume of ˜40 mL. The residue was diluted with 60 mL of methyl tert-butyl ether. This solution was then directly used for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188090B2
Source datasetuspto-grants-2012_05
ORD IDord-2c5eae8db22942c5bb0d451f01d2e2d6
Source noteuspto-grants-2012_05