HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → Tert-butyl 2-(4-amino-3-bromophenyl)morpholine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | tert-Butyl 2-(4-aminophenyl)morpholine-4-carboxylate | HCID 58315596 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 2-(4-amino-3-bromophenyl)morpholine-4-carboxylate | HCID 71743185 | 101.7% |
Reaction Steps
To a stirred solution of tert-butyl (RS)-2-(4-aminophenyl)morpholine-4-carboxylate (3.07 g, CAS-1002726-96-6) in DMF (30 ml) was added NBS (1.96 g) and the mixture was stirred at room temperature for 15 min. The reaction mixture was then poured into EtOAc and extracted sequentially with water and with saturated brine. The organic layer was dried over Na2SO4 and then concentrated in vacuo to afford tert-butyl (RS)-2-(4-amino-3-bromophenyl)morpholine-4-carboxylate (4.0 g, quant.) as a light brown solid which was used in the next step without further purification. MS (ISP): 359.0 ([{81Br}M+H]+), 357.0 ([{79Br}M+H]+), 303.0 ([{81Br}M+H—C4H8]+), 301.0 ([{79Br}M+H—C4H8]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09029370B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-5d1e57c5c3354146bac731a9303dac9d |
| Source note | uspto-grants-2015_05 |