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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052563Generated: October 30, 2026

Chlorosuccinimide → HCID 20351125, compound

https://huagongshe.com/reaction/2052563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 14708632HCID 14708632—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 20351125HCID 20351125—

Reaction Steps

A solution of 3-methylthiooxindole (1.70 g, 0.0095 mol) and N-chlorosuccinimide (1.34 g, 0.01 mol) in 100 ml of carbon tetrachloride was stirred at room temperature for 1 hour, the precipitate of succinimide was removed by filtration, and the filtrate was evaporated, yielding crude 3-chloro-3-methylthiooxindole. The residue, which was thus obtained, was dissolved in a minimum of tetrahydrofuran and added to a vigorously stirred slurry of red mercuric oxide powder (2.17 g, 0.01 mol) and boron trifluoride etherate (1.43 g, 0.01 mol) in 20 percent aqueous tetrahydrofuran (70 ml). After stirring at room temperature for 1 hour, 200 ml of ether was added, the reaction mixture was filtered through a pad of Celite and the organic phase of the filtrate was separated, dried over anhydrous magnesium sulfate, filtered, and this filtrate was evaporated to give isatin (1.07 g, 78%), mp 200°-202° after recrystallization from benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04186132
Source datasetuspto-grants-1980_01
ORD IDord-502fb93ddae449ee8f4785954a5dad47
Source noteuspto-grants-1980_01