HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromophenol → 2-[(4-Bromophenoxy)methyl]-2-methyloxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Chloromethyl)-2-methyloxirane | HCID 95220 | — |
| Product | 2-[(4-Bromophenoxy)methyl]-2-methyloxirane | HCID 66336120 | — |
Reaction Steps
4-Bromophenol (80 g, 462 mmol), 2-(chloromethyl)-2-methyloxirane (400 ml) and potassium carbonate (95.86 g, 693 mmol) were mixed and allowed to react at 100° C. for 4 hours. After the reaction was completed, the mixture was concentrated under reduced pressure. Ethyl acetate (200 ml) and water (400 ml) were added thereto, followed by extraction. The water layer was extracted with ethyl acetate (200 ml). The organic layer was washed with water (200 ml) twice. The organic layer was then concentrated under reduced pressure to remove the ethyl acetate. Thereafter, toluene was added and the resulting mixture was concentrated under reduced pressure, obtaining 120 g of crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598358B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-023e6a7af9ab4b9580fc9acc9b99ab86 |
| Source note | uspto-grants-2013_12 |