HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → HCID 6483409, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 135525222 | HCID 135525222 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 6483409 | HCID 6483409 | 80% |
Reaction Steps
Equimolecular amounts of (III), 2-phenyl-ethyl bromide and K2CO3 were refluxed in acetone for 48 h. The mixture was concentrated to small volume and shaken with diethyl ether and water. The ether phase was washed with 2 M NaOH, then with water, evaporated to dryness and the residue was recrystallized from ethanol. The title product was obtained in an 80% yield (abbreviation ON-6), m.p. 93-940° C. (ethanol); IR (KBr) 2227 (CN) cm1; 1H NMR (CDCl3) (δ, ppm) 2.66 (s, 3H, SCH3); 3.14 (t, 2H, CH2—Ph); 4.26 (t, 2H, O—CH2); 7.30 (m, 5H, arom.); 6.99-8.00 (m, 4H, arom.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06414004B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-256d619071ed4830aebb4e85f484e208 |
| Source note | uspto-grants-2002_07 |