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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448906Generated: October 30, 2026

Chlorosuccinimide → HCID 20351119, compound

https://huagongshe.com/reaction/1448906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant40800-69-9HCID 326650—
SolventChloroformHCID 6212—
ProductHCID 20351119HCID 20351119—

Reaction Steps

A solution of 3-methylthio-5-nitrooxindole (900 mg, 4 mmol) and N-chlorosuccinimide (600 mg, 4.5 mmol) in 50 ml of chloroform was stirred at room temperature for 1 hour and then evaporated to dryness in vacuo, yielding 3-chloro-3-methylthio-5-nitrooxindole. The residue was dissolved in 15 ml of tetrahydrofuran and added to a vigorously stirred slurry of red mercuric oxide powder (900 mg, 4.3 mmol) and boron trifluoride etherate (600 mg, 4.3 mmol) in 100 ml of 20 percent aqueous tetrahydrofuran. After stirring at room temperature for two hours, the reaction mixture was extracted with three 100-ml portions of chloroform. The chloroform layer was dried over anyhdrous magnesium sulfate, filtered and evaporated. The residue was recrystallized from 95 percent ethanol to give 5-nitroisatin (600 mg, 78%), mp 252°-254°

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04188325
Source datasetuspto-grants-1980_02
ORD IDord-cef6ba1f18734b02af7c968bf9a3c333
Source noteuspto-grants-1980_02