HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 19753816, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(Methylamino)propanoic acid, N-BOC protected | HCID 2760952 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19753816 | HCID 19753816 | 88.6% |
Reaction Steps
To a mixture of N-t-butoxycarbonyl-N-methyl-β-alanine (6.097 g) and triethylamine (4.18 ml) in ethyl acetate (60 ml) was added 2-bromoacetophenone (5.972 g) portionwise at 0°-5° C. After being stirred over night at ambient temperature, the solvent was evaporated and the resulting residue was dissolved in ethyl acetate (200 ml). The solution was washed with 0.5N hydrochloric acid (200 ml), water (200 ml) aqueous sodium bicarbonate (200 ml), water (200 ml) and brine (200 ml) successively, and dried over magnesium sulfate. Evaporation of the solvent gave N-t-butoxycarbonyl-N-methyl-β-alanine phenacyl ester (8.54 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04921855 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-12502f799d69486cb02dfc54d85447c7 |
| Source note | uspto-grants-1990_05 |