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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426146Generated: November 2, 2026

(+/-)-3-Methyl-5'-nitro-spiro[imidazolidine-4,2'-indane]-2,5-dione → (R)-3-Methyl-5'-nitro-spiro[imidazolidine-4,2'-indane]-2,5-dione

https://huagongshe.com/reaction/2426146

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+/-)-3-Methyl-5'-nitro-spiro[imidazolidine-4,2'-indane]-2,5-dioneHCID 18440305—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
SolventDiethylamineHCID 8021—
Product(R)-3-Methyl-5'-nitro-spiro[imidazolidine-4,2'-indane]-2,5-dioneHCID 67016436—

Reaction Steps

(±)-3-Methyl-5′-nitro-spiro[imidazolidine-4,2′-indane]-2,5-dione (described in Intermediate 7) was dissolved in a mixture of MeOH, CH3CN and diethylamine and the enantiomers were resolved by HPLC, utilizing a ChiralPak AD column and eluting with CH3CN:MeOH—90:10. The first major peak to elute was (S)-3-methyl-5′-nitro-spiro[imidazolidine-4,2′-indane]-2,5-dione and the second major peak to elute was (R)-3-methyl-5′-nitro-spiro[imidazolidine-4,2′-indane]-2,5-dione, the title compound. MS: m/z=262 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968540B2
Source datasetuspto-grants-2011_06
ORD IDord-090d43e67c0e498ba2bb2e83145aad02
Source noteuspto-grants-2011_06