HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → HCID 131718211, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 70053702 | HCID 70053702 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131718211 | HCID 131718211 | 51% |
Reaction Steps
The amine salt (0.34 g, 1.4 mmol), phenethyl bromide (0.26 g, 1.4 mmol), and potassium carbonate (0.50 g) were heated at reflux in absolute ethanol (50 mL) for 48 hours. After cooling, the mixture was filtered and concentrated in vacuo. The crude product was purified by chromatography on silica gel, eluting with 10% methanol in chloroform, and concentrated in vacuo to yield a colorless oil (0.25 g, 51%). 1H NMR(300 MHz, CDCl3 /TMS, δ): 7.45-7.10(m,10H), 4.36(s,2H), 3.6(t,2H,J=6Hz), 3.04-1.20(m,15H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05252586 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-0c1dafa4695043dab16c78e5fa2bc3d9 |
| Source note | uspto-grants-1993_10 |