Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenacylamine | HCID 11952 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ether tetrahydrofuran | HCID 21868444 | — |
| Reactant | HCID 178418816 | HCID 178418816 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21841526 | HCID 21841526 | — |
Reaction Steps
After dissolving 44.4 mmol of isobutylmagnesium bromide (2M ether solution) in 30 ml of a solvent mixture: ether/THF=1:1, a solution containing 2.0 g (14.8 mmol) of 2-aminoacetophenone in 10 ml of THF was added dropwise while maintaining the internal temperature at 15° C. or less. After stirring at 15° C. for an hour, the reaction mixture was poured into a saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 2.9 g of the desired product as an yellow oil. Yield was quantitative.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05914344 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-3752248536144c4daacb1482bb88050d |
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| Source note | uspto-grants-1999_06 |
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