HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650075Generated: October 30, 2026
Sodium Chloride → Ethyl [2-(benzyloxy)ethoxy]acetate
https://huagongshe.com/reaction/650075
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 2-(Benzyloxy) ethanol | HCID 12141 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl [2-(benzyloxy)ethoxy]acetate | HCID 54389372 | 30.8% |
Reaction Steps
A mixture of ethylene glycol monobenzyl ether (36 ml, 252 mmol), 60% sodium hydride (11.0 g, 275 mmol) and N,N-dimethylformamide (300 ml) was stirred at room temperature for 1.5 hours. To the resulting suspension was added dropwise a solution of ethyl bromoacetate (34 ml, 302 mmol) in N,N-dimethylformamide (50 ml), followed by stirring at room temperature for another 3 hours. The reaction mixture was poured into a 10% aqueous sodium chloride solution and extracted with ethylacetate, and the extract solution.was washed with a 5% aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent: ethyl acetate:n-hexane=9:95) to obtain 18.5 g of ethyl (2-benzyloxyethoxy)acetate as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06271251B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-a0275817f5854e6297f8831dc4d958f6 |
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| Source note | uspto-grants-2001_08 |
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