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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183564Generated: October 30, 2026

Methanol → HCID 178473123, compound

https://huagongshe.com/reaction/2183564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl bromopyruvateHCID 66144—
ReactantHCID 178423448HCID 178423448—
SolventAcetoneHCID 180—
ProductHCID 178473123HCID 17847312388%

Reaction Steps

A solution of 2-mercapto-5-methylbenzimidazole (200 mg, 1.22 mmol) and ethyl 3-bromopyruvate (0.20 mL, 1.43 mmol) in methanol (2 mL) and acetone (3 mL) was shaken at room temperature for 4 hours. The solvents were removed under the reduced pressure on a rotary evaporator. The residue was triturated with ethyl acetate. Solvent was decanted and the residue was dissolved in methylene chloride. The solution was washed with diluted aqueous sodium bicarbonate solution and water, and then dried over magnesium sulfate. Removal of the solvent gave the expected product, 3-(5-methoxy-1H-benzoimidazol-2-ylsulfanyl)-2-oxo-propionic acid ethyl ester (300 mg, 88%). 1H-NMR (D3COD, 300 MHz) δ (ppm): 7.19 (br. s, 1H), 7.10 and 7.04 (br. 2 s, 1H), 6.94 (d, J=8.2 Hz, 1H), 4.34 (q, J=7.1 Hz, 2H), 4.31 (br. s, 1H), 3.91 (br. s, 1H), 2.37 (br. s, 3H), 1.26 (t, J=7.1 Hz, 3H). MS (ESI): m/z 279 (M+1, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900218B2
Source datasetuspto-grants-2005_05
ORD IDord-a32e1a5e9e1640d6bc3d18ad6ddb12c7
Source noteuspto-grants-2005_05