HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetyl bromide → HCID 131727451, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Carbamic acid, [(1S)-2-(ethylamino)-1-methylethyl]-, 1,1-dimethylethyl ester | HCID 99965190 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131727451 | HCID 131727451 | — |
Reaction Steps
To a cold (0° C.) stirred solution of tert-butyl[(1S)-2-(ethylamino)-1-methylethyl]carbamate (11.0 g, 54.6 mmol) in a mixture of ethyl acetate (107 mL) and saturated aqueous sodium bicarbonate (65 mL), bromoacetyl bromide (12.1 g, 60.0 mmol) was added portionwise under an atmosphere of nitrogen. The mixture was allowed to warm up to room temperature over a period of 3.5 hours. The organic phase was separated, washed successively with saturated aqueous sodium bicarbonate, and brine. The organic extract was dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue was concentrated as a solution in toluene under vacuum to afford the title compound. ES MS M+1=323, 325.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538112B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-64dd112132bb4c36a34ed600cbca2250 |
| Source note | uspto-grants-2009_05 |