HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160310Generated: October 26, 2026
Ethyl trimethylsilylacetate → Ethyl 3-(4-fluorophenyl)-3-(4-hydroxyphenyl)-acrylate
https://huagongshe.com/reaction/1160310
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl trimethylsilylacetate | HCID 77687 | — |
| Reactant | 4-Fluoro-4'-hydroxybenzophenone | HCID 117666 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 3-(4-fluorophenyl)-3-(4-hydroxyphenyl)-acrylate | HCID 68674988 | 53.3% |
Reaction Steps
A solution of lithium hexamethyldisilazide (23.1 mL, 1 M in THF) was added to a stirred solution of ethyl (trimethylsilyl)acetate (2.53 mL, 13.9 mmol) in THF (15 mL) in 10 min. at −78° C. The reaction mixture was further stirred at this temperature for 20 min. A solution of (4-fluorophenyl)-(4-hydroxyphenyl)-methanone (2 g, 9.2 mmol) in THF (30 mL) was slowly added to the reaction mixture. The reaction mixture was brought to 0° C. in 5 h. The reaction mixture was quenched with saturated ammonium chloride solution, extracted into ethyl acetate and washed with dilute ammonium chloride solution. The organic layer was dried over magnesium sulfate. The solvent was removed under vacuum and product was purified flash chromatography on silica gel, giving 45.1 as an oil (1.405 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816367B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-3db90a0cb721452bb57d31ec9e0cfb42 |
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| Source note | uspto-grants-2010_10 |
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