Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl diethoxyacetate | HCID 80169 | — |
| Reactant | HCID 178436322 | HCID 178436322 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66724860 | HCID 66724860 | — |
Reaction Steps
Under an argon atmosphere, to a solution of ethyl diethoxyacetate (1.80 mL, 10.1 mmol) in THF (20 mL) was added slowly a THF solution (42) of (4-ethylbenzyl)magnesium chloride prepared above at −78° C. After stirring at −78° C. for an hour, to this was added 20% aqueous solution of ammonium chloride (10 mL), and the product was extracted with ethyl acetate (×3). The organic layer was sequentially washed with water (×1) and saturated brine (×1), and dried over anhydrous sodium sulfate. After filtration, the mixture was concentrated under reduced pressure and the residue was purified by silica gel flash column chromatography (n-hexane/ethyl acetate=9/1) to give 1,1-diethoxy-3-(4-ethylphenyl)propan-2-one (43) as a colorless oily substance (1.29 g, 5.04 mmol, 50.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546568B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-e96c2336f9ba481ea7222f6b853507ca |
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| Source note | uspto-grants-2013_10 |
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