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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | N,N-Bis(trimethylsilyl)trifluoroacetamide | HCID 65279 | — |
| Reactant | 2',3'-Dihydro-2H,5H-spiro[imidazolidine-4,1'-indene]-2,5-dione | HCID 233815 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3'-Bromo-2',3'-dihydro-2H,5H-spiro[imidazolidine-4,1'-indene]-2,5-dione | HCID 13563090 | 29% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04556670 |
|---|
| Source dataset | uspto-grants-1985_12 |
|---|
| ORD ID | ord-09007e70277143719c4560363768f66f |
|---|
| Source note | uspto-grants-1985_12 |
|---|