HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217976Generated: October 30, 2026
Ethyl bromoacetate → HCID 58406051, compound
https://huagongshe.com/reaction/217976
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 58406051 | HCID 58406051 | — |
Reaction Steps
Sodium hydride (2.5 g) was added to a solution of the compound obtained in Preparation Example 8-(3) (4.15 g) in 1-methyl-2-pyrrolidinone (60 mL) under ice-cooling. The reaction solution was stirred at the same temperature for 30 minutes. Ethyl bromoacetate (10.4 mL) was added dropwise to the reaction solution. The reaction solution was heated to room temperature and stirred at the same temperature for five hours. Saturated aqueous ammonium chloride and ethyl acetate were added to the reaction solution, and the organic layer was separated. The organic layer was washed with aqueous sodium chloride and then dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound (4.77 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198269B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-a8a079e6fba34c9489854b5e03505d25 |
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| Source note | uspto-grants-2012_06 |
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