HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → Ethyl 2-[4-(2-bromoethyl)-3-chlorophenoxy]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(2-Bromoethyl)-3-chlorophenol | HCID 22459408 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 2-[4-(2-bromoethyl)-3-chlorophenoxy]acetate | HCID 12049887 | — |
Reaction Steps
To a stirred solution of 4-(2-bromoethyl)-3-chlorophenol (158 mg) in acetone (7 ml) were added potassium carbonate (139 mg) and ethyl bromoacetate (89 μl) at room temperature. After the mixture was stirred for 20 hours at room temperature, the insoluble material was filtered off and the filtrate was concentrated in vacuo. Purification of the residue by medium pressure liquid column chromatography on silica gel (eluent: hexane/ethyl acetate 7/1) gave ethyl 2-[4-(2-bromoethyl)-3-chlorophenoxy]acetate (193 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399660B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-2f99117a4a784d0b802a708cedd321aa |
| Source note | uspto-grants-2002_06 |