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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596661Generated: October 25, 2026

Hydrochloric Acid → 1-(2-Chloro-6-fluorophenyl)-5-methylindolin-2-one

https://huagongshe.com/reaction/1596661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant2-chloro-N-(2-chloro-6-fluorophenyl)-N-(4-methylphenyl)acetamideHCID 4672920—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichlorobenzeneHCID 7239—
Product1-(2-Chloro-6-fluorophenyl)-5-methylindolin-2-oneHCID 11242841—

Reaction Steps

A mixture of 100 g (0.32 mol) of N-(2′-chloro-6′-fluorophenyl)-N-chloroacetyl-4-methylaniline and 110 g (0.82 mol) of aluminum chloride in 400 ml of 1,2-dichlorobenzene is stirred vigorously and heated to 140° for 7.5 hours. The reaction is cooled to room temperature and added to a mixture of 100 ml of 12N HCl and 700 ml of water (cooled to 0-5° in a dry ice/acetone bath). The mixture is extracted twice with 400 ml of methylene chloride and the combined organic layers are washed with 600 ml of 3N HCl. The organic layer is stirred with 66 g of magnesium sulfate and 33 g of charcoal (DARCO G-60). The solids are filtered through a pad of Celite and the solvents are evaporated under reduced pressure to give a tan solid which is recrystallized from ethanol to give N-(2′-chloro-6′-fluorophenyl)-5-methyloxindole, m.p. 137-140°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291523B1
Source datasetuspto-grants-2001_09
ORD IDord-297cb6bcd54b411f85f5dd6359e76437
Source noteuspto-grants-2001_09