HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723175Generated: November 1, 2026
Ethyl bromoacetate → HCID 14303535, compound
https://huagongshe.com/reaction/1723175
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2(3H)-Benzofuranone, 5-chloro-3-phenyl- | HCID 2876746 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14303535 | HCID 14303535 | — |
Reaction Steps
A solution of 42.8 mmol of 5-chloro-2,3-dihydro-2-oxo-3-phenylbenzofuran in 50 ml of anhydrous dimethylformamide is added at room temperature to a suspension of 42.8 mmol of sodium hydride in 20 ml of anhydrous dimethylformamide. The mixture is stirred for one hour at 20° C. and 42.8 mmol of ethyl bromoacetate are added. The mixture is stirred for 12 hours at 20° C., the medium concentrated under vacuum, the residue taken up in 200 ml of 1% strength hydrochloric acid solution, the aqueous phase extracted with benzene, the organic phase dried over anhydrous sodium sulfate, the solvent evaporated off and the crystalline residue washed with a solution of ethyl ether and acetone (90:10). After filtration, 25.8 mmol of crystals are collected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04859700 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-b492761ff00c4b2c8b476e1201508d11 |
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| Source note | uspto-grants-1989_08 |
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