HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-2-ethylbenzene → HCID 93510923, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-2-ethylbenzene | HCID 16089 | — |
| Reactant | (2R)-2-Ethyloxirane | HCID 11147670 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 93510923 | HCID 93510923 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
The 1-bromo-2-ethylbenzene (2.0 g) was dissolved in dry THF and the mixture was cooled to −78° C. 1.6 M n-BuLi (20.26 ml) was slowly added to the reaction mixture and then the mixture was stirred at −78° C. After 1 h (R)-(+)-1,2-epoxybutane (1.1 g) was added in 10 ml of THF. The reaction mixture was allowed to warm to ambient temperature and then stirred over night. The reaction was quenched with ice-water and product extracted in heptanes, and finally purified by using the separation method E yielding the title compound (1.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249127B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-01c265e2467949fd9ee20c95a63f0c7b |
| Source note | uspto-grants-2016_02 |