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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638541Generated: October 31, 2026

Ethyl bromoacetate → HCID 19836754, compound

https://huagongshe.com/reaction/1638541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant2-Nitrobenzyl alcoholHCID 11923—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
ProductHCID 19836754HCID 19836754—

Reaction Conditions

Temperature150 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880799
Source datasetuspto-grants-1989_11
ORD IDord-1036d742fd644d2daff7e06a9c845a7b
Source noteuspto-grants-1989_11