HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 54510282, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 19848363 | HCID 19848363 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54510282 | HCID 54510282 | 88% |
Reaction Steps
35.5 g (95 mmol) of 3-hydroxy-2,4,6-tribromobenzamide is suspended in 150 ml of methanol and dissolved by adding 2.18 g (95 mmol) of sodium. The mixture is combined with 17.5 g (104 mmol) of ethyl bromoacetate and maintained under reflux for three hours. After several hours of agitation, the crystallized product is vacuum-filtered, washed with a small amount of ice-cold methanol, and dried at b 60° C., thus obtaining 37.2 g (88% of theory) of 3-carbamoyl-2,4,6tribromophenoxyacetic acid methyl ester, mp 231°-233° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04869913 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-c56307b829d142da8d2617642903d4a9 |
| Source note | uspto-grants-1989_09 |