HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721431Generated: November 3, 2026
N,N-Dimethylaniline → 5-Allyl-2,3-dihydro-4-hydroxy-3,3-dimethyl-1H-indol-2-one
https://huagongshe.com/reaction/1721431
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | 4-Allyloxy-2,3-dihydro-3,3-dimethyl-1H-indol-2-one | HCID 22414873 | — |
| Product | 5-Allyl-2,3-dihydro-4-hydroxy-3,3-dimethyl-1H-indol-2-one | HCID 22414835 | — |
Reaction Steps
914 mg (4.21 mmol) of 4-allyloxy-2,3-dihydro-3,3-dimethyl-1H-indol-2-one was added to 4 ml of N,N-dimethylaniline, and the mixture was heated for 30 hours at 205° C. while stirring. After the reaction, N,N-dimethylaniline was evaporated under reduced pressure. The residue was dissolved in chloroform, washed with water, 2N hydrochloric acid, and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue obtained was purified by column chromatography (silica gel, chloroform:ethyl acetate=20:1), washed with ether-n-hexane, and filtered to obtain 890 mg (yield: 97.4%) of a brown oil of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05510366 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-8cfa9e4b48b6408b82f9e6f333330107 |
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| Source note | uspto-grants-1996_04 |
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