HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905727Generated: October 26, 2026
Acetyl chloride → N-(2-oxoindolin-5-yl)acetamide
https://huagongshe.com/reaction/905727
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 5-Amino-2-oxindole | HCID 2773213 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2-oxoindolin-5-yl)acetamide | HCID 11206280 | 88.9% |
Reaction Steps
A stirred solution of 5-amino-1,3-dihydro-indol-2-one (3.5 g, 23.6 mmol, prepared according to U.S. Pat. No. 6,114,371) in 20 ml of tetrahydrofuran was added with triethylamine (1.3 ml, 9 mmol). The solution was cooled down to −30° C. in an acetone-dry ice bath and added with acetyl chloride (1.3 ml, 9 mmol) dropwise. Upon the completion of the addition, the resulting mixture was stirred for 20 minutes at room temperature and added with ethyl acetate (20 ml) until precipitate was formed. The solid was filtered, washed with water (50 ml×3) and dried in vacuo to give N-(2-oxo-2,3-dihydro-1H-indol-5-yl)-acetamide (4 g, 88.9%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012966B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-8856ee18646342c1b70ad9e86dfefd07 |
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| Source note | uspto-grants-2011_09 |
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