HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377481Generated: October 30, 2026
Trifluoroacetic acid → HCID 57424264, compound
https://huagongshe.com/reaction/2377481
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 57424263 | HCID 57424263 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57424264 | HCID 57424264 | 88% |
Reaction Steps
A solution of 4-(2-bromo-4-methoxy-phenyl)-4-oxo-butyric acid ethyl ester (Intermediate 150, 6.45 g, 20.5 mmol) in trifluoroacetic acid (32 mL, 409 mmol) was treated with triethylsilane (14.4 mL, 90 mmol) and the resulting reaction mixture was heated at 55° C. for 3 h. The reaction mixture was then cooled to ambient temperature, neutralized with solid sodium bicarbonate, diluted with water and extracted with diethyl ether. The organic phase was washed with water and brine, dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo to afford the title compound (5.4 g, 88%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07468391B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-cc18466c943c4a9eba7c8936effdfbfb |
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| Source note | uspto-grants-2008_12 |
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