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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580012Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 13885779, compound

https://huagongshe.com/reaction/580012

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13885770HCID 13885770—
SolventDichloromethaneHCID 6344—
ProductHCID 13885779HCID 13885779—

Reaction Steps

A solution of 1.0 g (1.9 mMole) ethyl (±)-1,4-dihydro-5-isopropoxy-2-phenylthiomethyl-4-(2-trifluoromethylphenyl)-1,6-naphthyridine-3-carboxylate (Example 3.d) in 30 ml dichloromethane is cooled to 0° C. and 0.4 g (2.1 mMole) 3-chloroperoxy-benzoic acid (90%) is added portionwise thereto. After 10 minutes at 0° C., an aqueous solution of sodium hydrogen carbonate is added dropwise thereto and the organic phase is separated off, washed with water and dried over anhydrous sodium sulphate. After distilling off the solvent, the residue obtained is recrystallized from ethyl acetate. There is obtained ethyl (±)-1,4-dihydro-5-isopropoxy-2-phenylsulphinylmethyl-4-(2-trifluoromethylphenyl)-1,6-naphthyridine-3-carboxylate in the form of colorless crystals; mp 206°-208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04751228
Source datasetuspto-grants-1988_06
ORD IDord-3ef7b0a030e548a891b7f8e5d7d6a9a6
Source noteuspto-grants-1988_06