HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412395Generated: November 4, 2026
m-Chloroperbenzoic acid → HCID 54383742, compound
https://huagongshe.com/reaction/2412395
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 53996076 | HCID 53996076 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 54383742 | HCID 54383742 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04492700 |
|---|
| Source dataset | uspto-grants-1985_01 |
|---|
| ORD ID | ord-94b19d0803a046308476b72f7902bd0c |
|---|
| Source note | uspto-grants-1985_01 |
|---|