HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508489Generated: October 28, 2026
Azobisisobutyronitrile → 3-Bromo-5-methoxy-2,3-dihydro-1H-inden-1-one
https://huagongshe.com/reaction/508489
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Methoxyindan-1-one | HCID 78787 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-Bromo-5-methoxy-2,3-dihydro-1H-inden-1-one | HCID 23250651 | — |
Reaction Steps
N-bromosuccinimide (12.1 g, 67.9 mmol) and 2,2′-azobisisobutyronitrile (0.1 g, 0.6 mmol) were added to a solution of 5-methoxy-1-indanone (10.0 g, 61.7 mmol) in carbon tetrachloride (104 mL). The reaction mixture was stirred for 3 hours at 85° C. and then allowed to cool to room temperature. The reaction mixture was filtered through Celite, which was then washed with CH2Cl2 (100 mL). The filtrate was washed with brine (50 mL), dried over MgSO4, and concentrated to afford the subtitle compound, which was used without further purification. MS calculated for C10H9BrO2+H: 241, observed: 241.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096520B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-5d9b1721f9fd4893a75aa0fddcd77244 |
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| Source note | uspto-grants-2015_08 |
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