HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855029Generated: October 30, 2026
2,4-Dihydroxybenzaldehyde → HCID 58934503, compound
https://huagongshe.com/reaction/855029
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dihydroxybenzaldehyde | HCID 7213 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 5,5,5-trifluoropent-2-enoate | HCID 15104041 | — |
| Product | HCID 58934503 | HCID 58934503 | 98% |
Reaction Steps
A mixture of 10 g (72.5 mmol) of 2,4-dihydroxybenzaldehyde, 15.3 mL (101.4 mmol) of ethyl 4-triflouromethylcrotonate, and 20 g (145 mmol) of potassium carbonate in 25 mL of anhydrous dimethylformmamide was heated to 90° C. for three h. After cooling to room temperature, the reaction was added to 500 mL of ethyl acetate. The organic phase was washed with brine three times, dried over anhydrous magnesium sulfate and concd in vacuo. Silica chromatography with EtOAc/hexane (3:7) gave 19.0 g (98%) of a yellow solid: 1H NMR (CDCl3/400 MHz) 7.63 (s, 1H), 6.85(d, J=8.8 Hz, 1H), 6.79(dd, J=8.8 Hz, 2.8 Hz, 1H), 6.70(d, J=2.8 Hz, 1H), 5.63(q, J=6.8 Hz, 1H), 4.31(m, 2H), 1.34(t, J=7.2 Hz, 3H). MS (ESI+) 289.1 (M+1, 100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07259266B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-f7654d4c5b4b4a7f8c061b9a5b789063 |
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| Source note | uspto-grants-2007_08 |
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