HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 2-bromo-5-phenylthiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Phenylthiophene | HCID 69999 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-bromo-5-phenylthiophene | HCID 2776313 | — |
Reaction Steps
Next, 3.21 g (20 mmol) of the thus synthesized 2-phenylthiophene was dissolved into 20 mL of methanol, and then to this solution was added a solution wherein 3.92 g (22 mmol) of N-bromosuccinimide (Wako Pure Chemicals Industries, Ltd.) was dissolved into 40 mL of methanol, to produce a white precipitation of 2-phenyl-5-bromothiophene immediately. This reaction solution was put into a refrigerator to ensure the production of the precipitation. This precipitation was filtered and then was sufficiently washed with a great deal of a mixture solution of equivalent amounts of water and methanol. The resultant was dried one day and night to obtain a white crystal (2.4 g) of 2-phenyl-5-bromothiophene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06355365B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-b56225e69065413792dffad8c708c17c |
| Source note | uspto-grants-2002_03 |