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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347903Generated: October 30, 2026

Ethyl Thioglycolate → HCID 21083973, compound

https://huagongshe.com/reaction/347903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl ThioglycolateHCID 12185—
ReactantSodium hydrideHCID 24758—
ReactantHCID 21083969HCID 21083969—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
ProductHCID 21083973HCID 21083973—

Reaction Steps

To a solution of ethyl 2-mercaptoacetate (0.6 mL, 5.5 mmol) in dry DMF (10 mL) under nitrogen and cooled with an ice bath was added sodium hydride (220 mg of 60% dispersion in oil, 5.75 mmol). After hydrogen evolution had ceased the cooling bath was removed and the reaction stirred at room temperature for 30 mins. A solution of Intermediate 1 (920 mg, 4.6 mmol) in DMF (5 mL) was added and the reaction stirred at room temperature for 3 h. The reaction was quenched with water (50 mL) and extracted with EtOAc (3×50 mL). The combined EtOAc layers were washed with brine (50 mL), dried (MgSO4) and concentrated in vacuo to give a mixture of the title compound and uncyclised ethyl 2-(3-benzoylpyridin-2-ylsulfanyl)acetate. This crude mixture was dissolved in EtOH (10 mL) and sodium ethoxide (10 mL of 0.5M solution in EtOH, 5.0 mmol) added. The reaction was stirred at room temperature for 45 mins after which time complete conversion of uncyclised material to title compound was observed. The reaction was diluted with EtOAc (50 mL), washed with water (20 mL), dried (MgSO4) and concentrated in vacuo. The crude product was purified by chromatography on silica (10% EtOAc in isohexane) to give the title compound as a white solid (780 mg, 60%). δH (CDCl3) 8.63 (1H, dd, J 4.5, 1.4 Hz), 7.78 (1H, dd, J 8.2, 1.5 Hz), 7.41 (3H, m), 7.33–7.32 (2H, m), 7.24 (1H, dd, J 8.2, 4.6 Hz), 4.18 (2H, q, J 7.1 Hz), 1.15 (3H, t, J 7.1 Hz) LCMS (ES+) RT 3.90 minutes, 284 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176215B2
Source datasetuspto-grants-2007_02
ORD IDord-c9252df97e654f21a985e46f7d765a7e
Source noteuspto-grants-2007_02