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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723025Generated: November 3, 2026

m-Chloroperbenzoic acid → HCID 14372495, compound

https://huagongshe.com/reaction/1723025

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 14372494HCID 14372494—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14372495HCID 14372495—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 5 ml. of tetrahydrofuran containing 170 mg. (0.71 mmol) of 8-(2-pyrimidylthio)quinoline was added 300 mg. of sodium bicarbonate and the mixture cooled to 0° C. m-Chloroperbenzoic acid (85%, 153 mg., 1.0 molar equivalent) in 5 ml. of the same solvent was added dropwise. After the addition was complete the reaction was allowed to warm to 25° C. and was stirred overnight. The reaction mixture was poured into a sodium bicarbonate solution and the product extracted with ethyl acetate. The organic layer was separated, dried over sodium sulfate and concentrated in vacuo. The residue was triturated with a small amount of ethyl acetate and filtered to yield title product, 84 mg., m.p. 152°-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859679
Source datasetuspto-grants-1989_08
ORD IDord-ef2f21f94b774b1787d7541356ece76b
Source noteuspto-grants-1989_08