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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481951Generated: November 3, 2026

Ethyl bromoacetate → HCID 59771764, compound

https://huagongshe.com/reaction/1481951

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 numberUS09410199B2
Source datasetuspto-grants-2016_08
ORD IDord-2fb4011516a44f9ba7b51d8e57250c6d
Source noteuspto-grants-2016_08