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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83985Generated: October 27, 2026

Diisopropylethylamine → 1-Methanesulfonyl-5-chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine]

https://huagongshe.com/reaction/83985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactantp-Chlorocinnamyl chlorideHCID 53728250—
Reactant1-Methanesulfonyl-5-chloro-spiro[indoline-3,3'-pyrrolidine]HCID 58137339—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product1-Methanesulfonyl-5-chloro-1'-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3'-pyrrolidine]HCID 6892423945.8%

Reaction Steps

To a solution of 1-methanesulfonyl-5-chloro-spiro[indoline-3,3′-pyrrolidine] (725 mg) in acetonitrile (40 ml) were added diisopropylethylamine (0.66 ml) and 4-chloro-cinnamyl chloride (467 mg). The resulting solution was stirred at room temperature for 12 hours, diluted with ethyl acetate, washed with water, brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by silica gel chromatography (eluent cyclohexane:ethyl acetate 6:4) to afford 1-methanesulfonyl-5-chloro-1′-[trans-3-(4-chlorophenyl)allyl]spiro[indoline-3,3′-pyrrolidine] (500 mg) which was characterised by its mass and NMR spectra. MS (ES+) 437/439 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846907B2
Source datasetuspto-grants-2014_09
ORD IDord-f5ab99287f9542cdba20a7f4ba0be9a6
Source noteuspto-grants-2014_09