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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2275695Generated: November 2, 2026

Ethyl bromoacetate → HCID 59771764, compound

https://huagongshe.com/reaction/2275695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantHCID 59771748HCID 59771748—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59771764HCID 59771764—

Reaction Steps

To a solution of 2-(1-azido-ethoxy)-ethanol (0.15 g, 1.14 mmol) in dry tetrahydrofuran (THF) (5 ml) was added NaH (60% dispersion, 0.08 g, 2 mmol) at 0° C. After 15 minutes, ethyl-2-bromoacetate (0.222 ml, 2 mmol) was added. The reaction was maintained at this temperature for 15 minutes and then warmed up to room temperature. The reaction was quenched by addition of saturated aqueous NaHCO3 (5 ml) after 1 hr. After a further period of 5 min, the mixture was partitioned between DCM (50 ml) and saturated aqueous NaHCO3 (50 ml). The aqueous layer was further extracted with DCM (50 ml). All the DCM extracts were combined, dried over MgSO4 and evaporated under reduced pressure. The title compound was obtained as an oil (0.162 g, 65.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09127314B2
Source datasetuspto-grants-2015_09
ORD IDord-670c97f5d70e4108880691c613ffc2e5
Source noteuspto-grants-2015_09