HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl [2-(4-acetylphenoxy)ethyl]carbamate → Benzyl-[2-(4-bromoacetylphenoxy)-ethyl]-carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl [2-(4-acetylphenoxy)ethyl]carbamate | HCID 19889128 | — |
| Reactant | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl-[2-(4-bromoacetylphenoxy)-ethyl]-carbamate | HCID 12986050 | 90% |
Reaction Steps
Benzyl-[2-(4-acetyl-phenoxy)-ethyl]-carbamate (10.2 g, 32.5 mmol) was dissolved in methylene chloride (100 ml) and methanol (50 ml), and tetrabutylamonium tribromide (15.7 g, 32.5 mmol) was added in one portion. The reaction mixture was stirred for about sixteen hours, and then quenched with water. The aqueous phase was extracted with ethyl acetate and then washed with saturated aqeous sodium bicarbonate, and saturated Na2S2O3. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo, and the resulting crude material was purified by column chromatography (silica gel; hexanes to 2:1 hexanes/ethyl acetate) to afford a colorless oil which solidified upon standing. (11.5 g, 90% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06566377B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-3c1b8d842502498b9b20d44a9e878581 |
| Source note | uspto-grants-2003_05 |