HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700213Generated: October 29, 2026
Hydrochloric Acid → 5-(Chloroacetyl)-1,3-dihydro-2H-indol-2-one
https://huagongshe.com/reaction/1700213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Oxindole | HCID 321710 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-(Chloroacetyl)-1,3-dihydro-2H-indol-2-one | HCID 2060576 | 98% |
Reaction Steps
2-Oxindole (6.7 g) was added to a stirred suspension of 23 g of aluminum chloride in 30 mL of dichloroethane in an ice bath. Chloroacetyl chloride (11.3 g) was slowly added and hydrogen chloride gas was evolved. After ten minutes of stirring, the reaction was warmed at 40 to 50° C. for 1.5 hours. Thin layer chromatography (ethyl acetate, silica gel) showed no remaining starting material. The mixture was cooled to room temperature and poured into ice water. The precipitate was collected by vacuum filtration, washed with water and dried under vacuum to give 10.3 g (98%) of 5-chloroacetyl-2-oxindole as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06350754B2 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-18e8b7e2bd0d49aaaf26ae8c4e884150 |
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| Source note | uspto-grants-2002_02 |
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