HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2186764Generated: October 30, 2026
Ethyl phenylacetate → HCID 10752615, compound
https://huagongshe.com/reaction/2186764
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl phenylacetate | HCID 7590 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 1-(Triphenylmethyl)pyridinium tetrafluoroborate | HCID 9909412 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10752615 | HCID 10752615 | 43.6% |
Reaction Steps
Ethyl phenylacetate (3.13 g, 19 mmol, 1.0 equiv) was added in a dropwise manner to a solution of LDA (19 mmol, 1 equiv) in THF (30 mL) at −78° C. The resultant solution was maintained at to −78° C. for 25 minutes, and then warmed to 0° C. for 10 minutes. Triphenylmethylpyridinium tetrafluoroborate (7.8 g, 19 mmol, 1.0 equiv) was added in one portion. The reaction mixture was allowed to warm to 23° C. overnight and then concentrated. The residue was partitioned between saturated aqueous ammonium chloride (50 mL) and ethyl acetate (50 mL). The layers were separated, and the aqueous layer was dried over magnesium sulfate and concentrated. The residue was purified by flash column chromatography (25% THF/hexanes) to afford ethyl α-phenylpyridylacetate (2.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06407120B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-471fa1d961fb4a26b588a39e6273582f |
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| Source note | uspto-grants-2002_06 |
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