HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375610Generated: October 30, 2026
Hydrogen Peroxide → HCID 10039448, compound
https://huagongshe.com/reaction/375610
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Isatin | HCID 7054 | — |
| Reactant | 2-Amino-3-chlorobenzoic acid | HCID 80807 | — |
| Reactant | 4,6-Dichloroanthranilic acid | HCID 290498 | — |
| Reactant | HCID 18353297 | HCID 18353297 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 10039448 | HCID 10039448 | — |
Reaction Steps
To a stirred suspension of 15 g of 4,6-dichloroanthranilic acid (prepared from the corresponding isatine: T. Sandmeyer Helv. Chim. Acta, 2:234 (1919), by oxidation with alkaline hydrogen peroxide, following the procedure described by Baker et al., J. Org. Chem., 17:141 (1952) for the synthesis of 3-chloroanthranilic acid) in 100 mL of toluene was added 20 g of 1-aza-2-methoxy-1-cycloheptene. The mixture was stirred for an hour at room temperature, followed by heating under reflux for 18 hours. Then the mixture was concentrated in vacuo and volatile material was removed at 130° C. at 1 torr. The dark brown residue was chromatographed using 8:1 chloroform-ethyl acetate to give 9 g of the desired material as a crystalline solid, m.p. 110° C.-112° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05486512 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-ef68880949b14d9a9fc2e31645dd8e5c |
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| Source note | uspto-grants-1996_01 |
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