HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71217Generated: October 29, 2026
Acetic Acid → (3,4,5-Trifluoro-2-hydroxyphenyl)acetic acid
https://huagongshe.com/reaction/71217
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Reactant | 1-(3,4,5-Trifluoro-2-hydroxyphenyl)ethanone | HCID 83397209 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Product | (3,4,5-Trifluoro-2-hydroxyphenyl)acetic acid | HCID 84673812 | — |
Reaction Steps
A mixture of 1-(3,4,5-trifluoro-2-hydroxyphenyl)ethanone (7.5 g), p-toluenesulfonic acid monohydrate (0.375 g), morpholine (10 mL) and sulfur (2.0 g) was stirred at 120° C. for 5 hr, and allowed to cool to room temperature, and hydrochloric acid (20 mL) and acetic acid (20 mL) were added to the reaction mixture. The reaction mixture was stirred at 100° C. for 3 hr, allowed to cool to room temperature, and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (6.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822699B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-fcd1fc34450442c0826d4632225c6ab5 |
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| Source note | uspto-grants-2014_09 |
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