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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727949Generated: October 30, 2026

Pivalaldehyde → E-6-chloro-3-(2,2-dimethyl-propylidene)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1727949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPivalaldehydeHCID 12417—
ReactantPyrrolidineHCID 31268—
Reactant6-Chloro-1,3-dihydroindol-2-oneHCID 736344—
SolventMethanolHCID 887—
ProductE-6-chloro-3-(2,2-dimethyl-propylidene)-1,3-dihydro-indol-2-oneHCID 57565943—

Reaction Steps

In a manner similar to the method described in example 1a, 6-chlorooxindole (0.88 g, 5 mmol) was reacted with 2,2-dimethyl-propionaldehyde (0.43 g, 5 mmol) (Aldrich), pyrrolidine (0.36 g, 5 mmol) in methanol to give a mixture of E- and Z-6-Chloro-3-(2,2-dimethyl-propylidene)-1,3-dihydro-indol-2-one. Purification by chromatography (EtOAc:hexanes=1:2) led to E-6-chloro-3-(2,2-dimethyl-propylidene)-1,3-dihydro-indol-2-one as an off-white foam (Yield 0.82 g, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-6c311f1e01c94eba9bfa212f0f3adfd7
Source noteuspto-grants-2009_02