HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974391Generated: November 1, 2026
Sulfuric Acid → Ethyl 3-(2,4-difluorophenyl)prop-2-enoate
https://huagongshe.com/reaction/974391
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | 2,4-Difluoroaniline | HCID 9709 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Catalyst | 1,5-Diphenylpenta-1,4-dien-3-one;palladium | HCID 154270 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3-(2,4-difluorophenyl)prop-2-enoate | HCID 53395691 | — |
Reaction Steps
51.6 g (0.40 mol) or 2,4-difluoroaniline are dissolved in 240 ml of glacial acetic acid. 45 ml (0.80 mol) of concentrated sulfuric acid are added slowly with cooling. The white suspension is diazotized at 12°-15° C. using a solution of 28.0 g (0.406 mol) of sodium nitrite in 70 ml of water. 1.2 g (0.0044 mol) of palladium bis(1,5-diphenyl-1,4-pentadien-3-one) (lit.: M. F. Rettig et al., Inorg. Synth. 17 (1977), 134) are added to the resultant yellow solution at 45° C. 40.5 g (0.405 mol) of ethyl acrylate are then added dropwise. The reaction is slightly exothermic, and the temperature slowly rises to about 60° C. The reaction mixture is stirred overnight with falling temperature and then poured into about 600 ml of ice-water. The waxy precipitate is extracted with 500 ml of diethyl ether. The ether phase is separated off, washed several times with ice-water and then dried using sodium sulfate. The ether is removed by distillation on a vacuum rotary evaporator. 51.2 g (60% of theory) of a waxy crystalline product which, after recrystallization from petroleum ether, melts at 40°-40.5° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05068371 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-3ce316eaa7264875bd10b824dbaa80cd |
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| Source note | uspto-grants-1991_11 |
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