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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432878Generated: October 25, 2026

Ethyl bromoacetate → Ethyl 2-thienyloxyacetate

https://huagongshe.com/reaction/1432878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium HydroxideHCID 14798—
ReactantThiophen-2-olHCID 10909502—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductEthyl 2-thienyloxyacetateHCID 1132137819.4%

Reaction Steps

To a solution of 2-hydroxy-thiophene (32 g, 320 mmol) in CHCl3 (500 mL) is added ethyl bromoacetate (53.4 g, 320 mmol). To the resulting solution is added a solution containing n-Bu4NHSO4 (25 g, 74 mmol) and NaOH (15.8 g, 394 mmol) in water (500 mL). After addition, the solution is stirred vigorously using mechanical stirring. The reaction is stirred for 12 hours. After this time, the layers are separated. The aqueous layer is extracted with CHCl3. The combined organic layers are washed with water and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated under vacuum. The resulting crude product is purified by column chromatography eluting with a gradient of 30%CH2Cl2:hexanes to 60%CH2Cl2:hexanes. The title compound (11.5 g, 62 mmol) is obtained as 1H NMR (CDCl3, 300 MHz) δ6.68 (dd, 1H), 6.60 (d, 1H), 6.22 (d, 1H), 4.62 (s, 2H), 4.30 (q, 2H), 1.31 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-c655edf4b0934b1986692f79e66d8f2b
Source noteuspto-grants-2009_11