HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromopent-2-yne → HCID 58333165, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromopent-2-yne | HCID 85399 | — |
| Reactant | Indium | HCID 5359967 | — |
| Reactant | 1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone | HCID 11594370 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58333165 | HCID 58333165 | — |
Reaction Steps
1-(5,6-Dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanone (2 g), 1-bromo-2-pentyne (1.1 ml) and indium (983 mg) were suspended in THF (15 mL) and H2O (45 mL) and stirred vigorously overnight. The reaction mixture was then diluted with water and ethyl acetate, the layers were separated and the aqueous layer was extracted with ethyl acetate. The combined extracts were washed with brine and dried over Na2SO4 to yield a crude material. The crude material was purified by column chromatography (SiO2; 5-30% ethyl acetate/hexanes) to yield the title compound as a peach-colored solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120830B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-3ab11a9dac6d4a868fb873347a83e448 |
| Source note | uspto-grants-2015_09 |