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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051485Generated: October 31, 2026

Methyl formate → HCID 178493211, compound

https://huagongshe.com/reaction/2051485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl formateHCID 7865—
ReactantSodium HydroxideHCID 14798—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178493200HCID 178493200—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178493211HCID 178493211—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-chloro-2-[[(3,4-dimethoxy-2-pyridinyl)methyl]thio]-1H-benzimidazole (645 mg, 0.0019 mol) was dissolved in 25 ml CH2Cl2 and mixed with NaHCO3 (323 mg, 0.0038 mol) dissolved in 10 ml H2O. The stirred mixture was cooled to 0° C. and treated with MCPBA (84%, 389 mg, 0.0019 mol) dissolved in 6 ml CH2Cl2. After reacting for 10 min the layers were separted and the aqueous layer extracted with 5 ml CH2Cl2. The organic layers wcre combined and extracted with 20 ml water containing NaOH (154 mg, 0.0038 mol). The latter aqueous layer was collected (residual CH2Cl2 distilled off on the rotavapor) and treated with two portions of HCOOCH3 (2×118 μl, 0.0038 mol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05019584
Source datasetuspto-grants-1991_05
ORD IDord-8f01cf67904343c0baeb2bf07437c85f
Source noteuspto-grants-1991_05