HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644709Generated: 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/1644709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(4-Fluorophenyl)acetic acid | HCID 9837 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Ethyl 2-(triphenylphosphoranylidene)propionate | HCID 79792 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Heptane | HCID 8900 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 4-(4-Fluoro-phenyl)-2-methyl-buta-2,3-dienoic acid ethyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124629B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-707499795d2d4c67b5812bb8f8bb595f |
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| Source note | uspto-grants-2012_02 |
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