HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476860Generated: October 31, 2026
Ethyl bromoacetate → HCID 19836754, compound
https://huagongshe.com/reaction/476860
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 2-Nitrobenzyl alcohol | HCID 11923 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19836754 | HCID 19836754 | — |
Reaction Steps
20 g o-nitro benzylalcohol and 21.7 ml ethyl bromoacetate was dissolved in 250 ml dry DMF. Portions of 55-60% sodium hydride were added to this solution under stirring over one hour until a total amount of 8.5 g had been added. The mixture was left overnight at room temperature and then heated to 150° C. under stirring for 2 hours. The mixture was then evaporated and the residue was partitioned between diethylether and water. The organic phase was evaporated to give 14 g ethyl (o-nitro-benzyloxy)acetate as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04886797 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-1b83a84a119a4bdfaf4b63abc32196be |
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| Source note | uspto-grants-1989_12 |
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