HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401699Generated: October 31, 2026
Acetone → 2-Hydroxy-4-(trifluoromethyl)benzaldehyde
https://huagongshe.com/reaction/2401699
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 86680838 | HCID 86680838 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxy-4-(trifluoromethyl)benzaldehyde | HCID 22493901 | 72.1% |
Reaction Steps
A mixture of 1.90 g of 2-ethoxymethoxy-4-trifluoromethylbenzaldehyde, 10 ml of acetone, and 9 ml of 6 N hydrochloric acid was stirred at room temperature for 3 hours and subsequently at 40° C. for 1 hour. The reaction mixture was cooled to room temperature, then water was added to the reaction mixture. This mixture was extracted twice with ethyl acetate. The organic layers were combined and washed with water and saturated brine and dried over magnesium sulfate, then concentrated under reduced pressure, to obtain 1.05 g of 2-hydroxy-4-(trifluoromethyl)benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08796306B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-7f89922f072549efae67753ae4381793 |
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| Source note | uspto-grants-2014_08 |
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