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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-chloro-N-(2-chloro-6-fluorophenyl)-N-(4-methylphenyl)acetamide | HCID 4672920 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | 1-(2-Chloro-6-fluorophenyl)-5-methylindolin-2-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06291523B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-297cb6bcd54b411f85f5dd6359e76437 |
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| Source note | uspto-grants-2001_09 |
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