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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059957Generated: October 25, 2026

Ethyl bromoacetate → ethyl 2-(1H-1,3-benzodiazol-2-ylsulfanyl)acetate

https://huagongshe.com/reaction/2059957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant2-MercaptobenzimidazoleHCID 707035—
SolventEthanolHCID 702—
Productethyl 2-(1H-1,3-benzodiazol-2-ylsulfanyl)acetateHCID 2156430,947.1%

Reaction Steps

To a stirred solution of 1H-benzo[d]imidazole-2(3H)-thione (20.0 g, 0.13 mol, 1.0 eq.) in anhydrous ethanol (500 mL) at room temperature, was added potassium carbonate (9.25 g, 0.07 mol, 0.5 eq.) and ethyl bromoacetate (26.7 g, 0.16 mmol, 1.2 eq.). The reaction was heated to reflux and stirred at that temperature for 6 hours. The solvent was removed in vacuo and water (200 mL) was added. The aqueous phase was extracted with dichloromethane (3×100 mL), and the combined organic extracts were washed with water (200 mL) and brine (200 mL). The organic phase was dried over magnesium sulfate and concentrated in vacuo to give a colorless oil which solidified on standing. Purification by flash chromatography (CHCl3→10% MeOH:90% CHCl3) gave 4a as a white solid (11.7 g, 37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278327B2
Source datasetuspto-grants-2012_10
ORD IDord-fd220d09049246eba6a85a82436efdbe
Source noteuspto-grants-2012_10