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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727947Generated: November 2, 2026

Pyrrolidine → Z-6-chloro-3-(3,3-dimethyl-butylidene)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1727947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
Reactant3,3-DimethylbutanalHCID 76335—
Reactant6-Chloro-1,3-dihydroindol-2-oneHCID 736344—
SolventMethanolHCID 887—
ProductZ-6-chloro-3-(3,3-dimethyl-butylidene)-1,3-dihydro-indol-2-oneHCID 86615083100%

Reaction Conditions

Temperature100 °C

Reaction Steps

To the mixture of 6-chlorooxindole (0.26 g, 1.49 mmol) (Crescent) and 3,3-dimethyl-butyraldehyde (0.21 g, 2.09 mmol) (Aldrich) in methanol (20 mL) was added pyrrolidine (0.15 g, 2.09 mmol) (Aldrich) dropwise. The mixture was then heated at 100° C. for 1 h. The mixture was concentrated, and the residue was partitioned between ethyl acetate and water. The organic layer was separated, dried over Na2SO4, concentrated, and dried in vacuo to give the crude E/Z-6-chloro-3-(3,3-dimethyl-butylidene)-1,3-dihydro-indol-2-one as a white solid (Yield 0.37 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-6f1ccc43c2244600ba1f8144cbf92c43
Source noteuspto-grants-2009_02