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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727953Generated: November 3, 2026

Sodium Hydroxide → racemic (2'R,3R,4'S)-6-chloro-2',4'-bis(3-chlorophenyl)spiro[3H-indole-3,3'-piperidine]-2,6'-dione

https://huagongshe.com/reaction/1727953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantracemic (2'R,3R, 4'S)-6-chloro-2',4'-bis(3-chlorophenyl)-2,3-dihydro-2,6'-dioxo spiro[indole-3,3'-piperidine]-1-carboxylic acid ethyl esterHCID 91457502—
SolventMethanolHCID 887—
Productracemic (2'R,3R,4'S)-6-chloro-2',4'-bis(3-chlorophenyl)spiro[3H-indole-3,3'-piperidine]-2,6'-dioneHCID 13172730651%

Reaction Steps

To a solution of racemic (2′R,3R,4′S)-6-chloro-2′,4′-bis(3-chlorophenyl)-2,3-dihydro-2,6′-dioxospiro[indole-3,3′-piperidine]-1-carboxylic acid ethyl ester prepared in example 4c (0.45 g, 0.92 mmol) in methanol (30 mL) was added NaOH (66 mg, 1.65 mmol). The mixture was stirred at room temperature for 0.5 h. The solvent was removed and the residue was partitioned between ethyl acetate and aqueous HCl solution (1 N). The aqueous layer was extracted with ethyl acetate. The organic layers were combined and then concentrated. The residue was purified with chromatography (EtOAc:CH2Cl2=1:3) to give racemic (2′R,3R,4′S)-6-chloro-2′,4′-bis(3-chlorophenyl)spiro[3H-indole-3,3′-piperidine]-2,6′-dione as a white solid (Yield 0.2 g, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-ed15fb58d76e4229b7762f540125087c
Source noteuspto-grants-2009_02