HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296496Generated: October 30, 2026
Ethyl bromoacetate → HCID 19848366, compound
https://huagongshe.com/reaction/2296496
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 19848356 | HCID 19848356 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19848366 | HCID 19848366 | 84.1% |
Reaction Steps
16 g (66.9 mmol) of 3-hydroxy-2,4,6-trichlorobenzamide is suspended in 100 ml of methanol and dissolved by adding 1.54 g (66.9 mmol) of sodium. After the addition of 16.8 g (66.9 mmol) of bromoacetic acid ethyl ester, the mixture is maintained under reflux until the reaction is complete (TLC control). The product is then concentrated to dryness under vacuum and the resultant 3-carbamoyl-2,4,6-trichlorophenoxyacetic acid methyl ester is suspended in 100 ml of water. The mixture is combined with 20 ml of concentrated sodium hydroxide solution and maintained for 3 hours at 60° C. for saponifying. The solution is filtered over active carbon, brought to pH 2 by adding concentrated hydrochloric acid, and the precipitate is vacuum-filtered after several hours of stirring in an ice bath. After washing with water and drying, 16.8 g (84% of theory) of 3-carbamoyl-2,4,6-trichlorophenoxyacetic acid is obtained as a white powder, mp 261°-262° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04429152 |
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| Source dataset | uspto-grants-1984_01 |
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| ORD ID | ord-0f6f7de4a12c4c118651fa634e2f78d3 |
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| Source note | uspto-grants-1984_01 |
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