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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
Reactant4-Allyloxy-2,3-dihydro-3,3-dimethyl-1H-indol-2-oneHCID 22414873—
Product5-Allyl-2,3-dihydro-4-hydroxy-3,3-dimethyl-1H-indol-2-oneHCID 22414835—

Reaction Conditions

Temperature205 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05510366
Source datasetuspto-grants-1996_04
ORD IDord-8cfa9e4b48b6408b82f9e6f333330107
Source noteuspto-grants-1996_04