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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665850Generated: November 2, 2026

Trifluoroacetic acid → HCID 12505004, compound

https://huagongshe.com/reaction/1665850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 57826337HCID 57826337—
SolventWaterHCID 962—
ProductHCID 12505004HCID 1250500478.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039634B2
Source datasetuspto-grants-2011_10
ORD IDord-ee074e53166f4133a18747b1dabd61d7
Source noteuspto-grants-2011_10