HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665850Generated: November 2, 2026
Trifluoroacetic acid → HCID 12505004, compound
https://huagongshe.com/reaction/1665850
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 57826337 | HCID 57826337 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12505004 | HCID 12505004 | 78.2% |
Reaction Steps
30 g (0.091 mol) of 2-(4-methoxyphenyl)-1-phenyl-2-trimethylsilanyloxy-ethanone prepared in Step 2 was added to 50 mL of an aqueous 90% trifluoroacetic acid solution and the resulting reaction solution was stirred at room temperature for 2 hours. An ice bath was placed and the resulting reaction solution was neutralized with addition of sodium carbonate. Then, 200 mL of ethyl acetate and 100 mL of water were added to dilute the solution, followed by separation of layers. The obtained organic layer was washed twice with 100 mL of a saturated sodium bicarbonate solution and then successively washed twice with 100 mL of a brine solution. The organic layer thus obtained was dried over magnesium sulfate, filtered and concentrated under reduced pressure to give 17.25 g of a final product which was then recrystallized from ethyl acetate and hexane, to give 14.38 g (yield: 65%) of pure 2-hydroxy-2-(4-methoxyphenyl)-1-phenyl-ethanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039634B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-ee074e53166f4133a18747b1dabd61d7 |
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| Source note | uspto-grants-2011_10 |
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