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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219776Generated: October 29, 2026

Ethyl bromoacetate → 3-[2-Azido-2-(2-ethoxycarbonylmethoxyethoxy)ethoxy]benzoic acid

https://huagongshe.com/reaction/2219776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactant3-[2-Azido-2-(2-hydroxyethoxy)ethoxy]benzoic acidHCID 59771766—
SolventTetrahydrofuranHCID 8028—
Product3-[2-Azido-2-(2-ethoxycarbonylmethoxyethoxy)ethoxy]benzoic acidHCID 5977177131.6%

Reaction Steps

To a solution of 3-[2-azido-2-(2-hydroxy-ethoxy)-ethoxy]-benzoic acid (0.535 g, 2 mmol) in dry THF (6 ml) was added NaH (60% dispersion, 0.246 g, 6 mmol) at 0° C. After 10 minutes, ethyl-2-bromoacetate (0.488 ml, 4.4 mmol) was added. The reaction was then warmed up to room temperature and stirred for 4 hours. The reaction was quenched by pouring it into ice-cold water (50 ml). The mixture was extracted with DCM (2×50 ml) and the DCM extracts were discarded. The aqueous layer was then acidified to pH 2 with 1 N HCl, and extracted with DCM (2×50 ml). These DCM extracts were combined, dried over MgSO4 and evaporated under reduced pressure. The residue was purified by column chromatography (1×20 cm). The title compound, eluted with 2% methanol in DCM, was obtained as an oil (0.223 g, 31.6%). ES-MS, m/z 351.95 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414116B2
Source datasetuspto-grants-2008_08
ORD IDord-30b81a7863dc4d3998e7b65f983d3020
Source noteuspto-grants-2008_08