HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580012Generated: November 2, 2026
m-Chloroperbenzoic acid → HCID 13885779, compound
https://huagongshe.com/reaction/580012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 13885770 | HCID 13885770 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13885779 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04751228 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-3ef7b0a030e548a891b7f8e5d7d6a9a6 |
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| Source note | uspto-grants-1988_06 |
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