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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085105Generated: October 26, 2026

Sodium Hydroxide → HCID 178527212, compound

https://huagongshe.com/reaction/1085105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178505473HCID 178505473—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178527212HCID 178527212—

Reaction Steps

5- Fluoro-2-[[(4-cyclopropylmethoxy-2-pyridinyl)methyl]-thio]-1H-benzimidazole (1.25 g, 0.0036 mol) was dissolved in CH2Cl2 (40 ml). NaHCO3 (0.6 g, 0.0072 mol) dissolved in H2O (20 ml) was added and the mixture was cooled to +2° C. m-Chloroperbenzoic acid, 84% (0.73 g, 0.0036 mol) dissolved in CH2Cl2 (5 ml) was added under stirring. Stirring was continued at room temperature for 15 min. The two phases were separated and NaOH (0.29 g, 0.0072 mol) dissolved in H2O (25 ml) was added to the organic phase. The mixture was stirred, the phases were separated and the H2O phase was treated with Norite and filtered. Methylformiate (0.45 ml, 0.0073 mol) dissolved in H2O (5 ml) was added dropwise under stirring. After extraction with CH2Cl2 and drying with Na2SO4 the solvent was evaporated. In this way the title compound was obtained (0.93 g, 69%). NMR data for the final product is given below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008278
Source datasetuspto-grants-1991_04
ORD IDord-86d387f429a44c588dca59b32aa1eaa8
Source noteuspto-grants-1991_04