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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637314Generated: October 31, 2026

Bromine → 3'-Bromo-2',3'-dihydro-2H,5H-spiro[imidazolidine-4,1'-indene]-2,5-dione

https://huagongshe.com/reaction/637314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantN,N-Bis(trimethylsilyl)trifluoroacetamideHCID 65279—
Reactant2',3'-Dihydro-2H,5H-spiro[imidazolidine-4,1'-indene]-2,5-dioneHCID 233815—
SolventChloroformHCID 6212—
Product3'-Bromo-2',3'-dihydro-2H,5H-spiro[imidazolidine-4,1'-indene]-2,5-dioneHCID 1356309029%

Reaction Conditions

Temperature25 °C

Reaction Steps

Spiro[imidazolidine-4,1'-indan]2,5-dione, (C.A. reg. no. 6252-98-8) (6.06 g, 30 mmol) was combined with 7.95 ml (30 mmol) bis(trimethylsilyl)trifluoroacetamide and 4.8 g (30 mmol) bromine in 50 ml chloroform and heated to reflux. Decolorization occurred during the 18 hour reaction. The reaction mixture was cooled to 25° C. and after 45 minutes stirring a solid which had crystallized was collected by filtration to give 2.45 g (29%) of crude 3'-bromo-spiro[imidazolidine-4,1'-indan]2,5-dione. The chloroform mother liquors deposited an additional 2.18 g (26% yield), mp 58°-65° C. Two grams (7.1 mmol) of material, mp 58°-65° C., was combined with 25 ml water to give a slurry. Following stirring for 22 hours the resultant solid was collected by filtration and dried to give 0.52 g (33% yield) of the title compound: mp 260°-263° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04556670
Source datasetuspto-grants-1985_12
ORD IDord-09007e70277143719c4560363768f66f
Source noteuspto-grants-1985_12