HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 22414392, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 22414442 | HCID 22414442 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22414392 | HCID 22414392 | 30.3% |
Reaction Steps
A stirred solution of 3.0 g of 2-amino-N-methyl-α-(2-methyl-3-thienyl)benzeneethanamine in 50 ml of N,N-dimethylformamide was treated with a solution of 2.6 g of N-bromosuccinimide in 50 ml of N,N-dimethylformamide and allowed to stand overnight at room temperature. Evaporation of the volatiles afforded an oil :which was purified by HPLC (Water's Associates Prep LC/System 500, silica gel, elution with methanol). The resultant oil was dissolved in diethyl ether, filtered and concentrated. Trituration with diethyl ether afforded 1.2 g of 2-amino-5-bromo-N-methyl-α-(2-methyl-3-thienyl)benzeneethanamine, mp 72.5°-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05510346 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-fee238ad39cf40caa009baa2ec06a2e5 |
| Source note | uspto-grants-1996_04 |