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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412395Generated: November 4, 2026

m-Chloroperbenzoic acid → HCID 54383742, compound

https://huagongshe.com/reaction/2412395

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 53996076HCID 53996076—
SolventChloroformHCID 6212—
ProductHCID 54383742HCID 54383742—

Reaction Conditions

Temperature0 °C

Reaction Steps

1.25 grams (0.005 mole) of N-benzylidene-2-chloropyrazine-3-sulfenamide in 25 milliliters of chloroform was added to a rapidly stirring mixture of 0.69 gram (0.25 millimole) of sodium bicarbonate and the resulting mixture cooled to 0° C. To the cooled solution, a solution of gram (5.5 millimole) of m-chloroperbenzoic acid in 25 milliliter of chloroform was added dropwise over a 15 minute period. After completion of the addition, stirring was continued for 15 hours. At the end of this period, chloroform layer was separated from the aqueous layer, dried over anhydrous potassium carbonate, and subjected to reduced pressure to remove the solvent and to recover as residue an oil which solidified on standing. The latter was purified by crystallization from ethanol to obtain the desired N-benzylidene-2-chloropyrazine-3-sulfinamide product, m.p. 113°-114° C. Elemental analyses were as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04492700
Source datasetuspto-grants-1985_01
ORD IDord-94b19d0803a046308476b72f7902bd0c
Source noteuspto-grants-1985_01