HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophene → HCID 12060894, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12060894 | HCID 12060894 | 34% |
Reaction Steps
To stirred solution of m-bromoaniline (34.4 g; 0.2M) in thiophene (200 mL) was added isoamylnitrite (46.86 g; 0.4M) dropwise over a period of 30 mins. at 0° C. The resulting mixture was cautiously warmed to R.T. and heated to reflux for 16 hours. The reaction mixture was cooled, diluted with 400 mL of ether, washed with 3×100 mL of satd. sodium chloride solution, and dried over anhydrous magnesium sulfate. Solvent and excess thiophene were removed. A solution of the residue in 200 mL of ether was filtered through 50 G silica gel bed. Solvent was removed, and the residue was distilled to give 34% of 2-(3'-bromophenyl)thiophene as a yellow liquid boiling at 130°-2°/~0.2 mm. This liquid solidified on standing in the refrigerator.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05143914 |
| Source dataset | uspto-grants-1992_09 |
| ORD ID | ord-ce1f23167bbc4e8281abd639a6e1f6cb |
| Source note | uspto-grants-1992_09 |