HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236377Generated: October 25, 2026
Acetyl chloride → 1-Ethyl-5-acetyloxindole
https://huagongshe.com/reaction/236377
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | N-Ethyloxindole | HCID 66135 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 1-Ethyl-5-acetyloxindole | HCID 13770531 | 57.3% |
Reaction Steps
To a mixture of 29.25 g. (0.373 mole) of acetyl chloride and 65.9 g. of aluminum chloride in 60 ml. of nitrobenzene was added gradually 20.0 (0.124 mole) of 1-ethyloxindole. The reaction warmed to about 45° C. with an evolution of gas. After stirring for one hour the reaction was heated to 100° C. for one hour and allowed to stir at room temperature over night. The reaction mixture was poured into 2 l. of ice with stirring. After 30 minutes the product was filtered, air dried and dissolved in 200 ml. of methylene chloride. The solution was dried over magnesium sulfate and concentrated to dryness. The residue was recrystallized from toluene, 14.44 g. (57.3% yield), m.p. 141°-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04644005 |
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| Source dataset | uspto-grants-1987_02 |
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| ORD ID | ord-cd5efd8eaf214fefa25af3f3f35f904d |
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| Source note | uspto-grants-1987_02 |
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