HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964365Generated: October 30, 2026
Ethyl bromoacetate → HCID 14988926, compound
https://huagongshe.com/reaction/964365
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 14988919 | HCID 14988919 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14988926 | HCID 14988926 | 71.3% |
Reaction Steps
To a solution of 4-[3-(2-hydroxyethyl)-2-methyloxiranyl]-5-methoxy-6-(morpholinocarbonyloxy)-1-oxaspiro[2,5]octane (76.2 mg) in a mixture of toluene (2 ml) and N,N-dimethylformamide (1 ml) was added sodium hydride (20.5 mg) in one portion under ice cooling. The mixture was stirred for half an hour at the same temperature and ethyl bromoacetate (68.5 mg) was added. After stirred for 3 hours at ambient temperature, the reaction mixture was quenched with aqueous saturated ammonium chloride solution (2 ml). The organic layer was washed with brine, dried, and evaporated in vacuo. The residue was purified by column chromatography on silica gel (diethyl ether) to give 4-[3-(2-ethoxycarbonylmethoxyethyl)-2-methyl-oxiranyl]-5-methoxy-6-(morpholinocarbonyloxy)-1-oxaspiro-[2,5]octane (66.9 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05767293 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-7d868978d97544eea8c1c812c4c3d8b8 |
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| Source note | uspto-grants-1998_06 |
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