Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 90060209 | HCID 90060209 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 118260105 | HCID 118260105 | 89% |
Reaction Steps
(S)-2-tert-Butoxycarbonylamino-3-(4-but-2-ynyloxy-phenyl)-propionic acid (380 mg) was dissolved in ethyl acetate (5.0 mL). A commercially available reagent of 2-bromoacetophenone (164 mg) and Et3N (115.7 μL) were added and the mixture was stirred at room temperature for 2 days. To the reaction solution was added ethyl acetate and the mixture was washed with water and a saturated brine in this order. The organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The product was purified by recrystallization in 15% ethyl acetate/n-hexane to obtain 2-oxo-2-phenyl-ethyl (S)-2-tert-butoxycarbonylamino-3-(4-but-2-ynyloxy-phenyl)-propionate (277 mg, yield 89% over 2 steps) as colorless crystal (LCMS m/z 452 (M+1) Rt 232 min.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266853B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-83ebd294e62045258463911101f16c93 |
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| Source note | uspto-grants-2016_02 |
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