HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484511Generated: October 31, 2026
4-Hydroxy-2-(trifluoromethoxy)benzaldehyde → HCID 68322507, compound
https://huagongshe.com/reaction/1484511
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxy-2-(trifluoromethoxy)benzaldehyde | HCID 24721507 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic acid ethanol | HCID 18476134 | — |
| Product | HCID 68322507 | HCID 68322507 | — |
Reaction Steps
A solution of 4-hydroxy-2-(trifluoromethoxy)benzaldehyde (210 g, 1 equiv) in ethanol: acetic acid 3:1 (1050 Lt) was treated with Pd/C 5% catalyst-50% wet (21 g) and stirred at 800 rpm under 5 bar of hydrogen for 2.5 hrs. A second aliquot of Pd/C 5% catalyst-50% wet (33.6 g) was then added and the mixture subjected to the same hydrogenation conditions until reaching 22 hrs in total. The reaction mixture was filtered on a charcoal cartridge and washed with ethanol (525 mL). The resulting clear solution was concentrated to ca. 420 mL and the residue diluted with ethyl acetate (1050 Lt) and an aqueous 10% solution of ammonium chloride (525 mL). The phases were allowed separating and the organic one washed with water (2×525 mL), dried over sodium sulfate, filtered and concentrated to dryness. The title compound was obtained as colorless oil (196 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422252B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-2930e7a3260548b1b2e2bedb8ccebebd |
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| Source note | uspto-grants-2016_08 |
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