HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromotrichloromethane → (Bromoethynyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromotrichloromethane | HCID 6383 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Catalyst | Phenylacetylene | HCID 10821 | — |
| Catalyst | Tetrabutylammonium Fluoride Trihydrate | HCID 11726816 | — |
| Product | (Bromoethynyl)benzene | HCID 136737 | 95% |
Reaction Steps
In a 10 mL round-bottom flask, 1.02 g of phenylacetylene (10 mmol), 2.1 g bromotrichloromethane (10.5 mmol) and 100 mg of tetra-n-butylammonium fluoride trihydrate (0.316 mmol) were stirred at 24° C. for 15 min. The temperature of the mixture rose to 33° C. in the course of the process. Analysis of the resulting mixture showed that it contained 1.72 g of 1-bromo-2-phenylacetylene (95% yield) and 0.05 g of the unconverted phenylacetylene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05132475 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-0484acd9f3944462977eedecda75db40 |
| Source note | uspto-grants-1992_07 |