HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077405Generated: November 2, 2026
4-bromo-N,N-dimethylaniline → HCID 19431307, compound
https://huagongshe.com/reaction/1077405
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-bromo-N,N-dimethylaniline | HCID 11465 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 19431303 | HCID 19431303 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19431307 | HCID 19431307 | — |
Reaction Steps
Magnesium (124 mg, 5.1 mmol) is covered with 1 ml of distilled THF and heated at 60° C. with stirring. A solution of 4-bromo-N,N-dimethylaniline (1.02 g, 5.1 mmol) in 5 ml of distilled THF is added dropwise over the course of 20 min. The reaction mixture is heated at reflux of the THF for 1 h. A solution of 5,6-di(tert-butyldimethylsilyloxy)indan-1-one (2 g, 5.1 mmol) in 10 ml of distilled THF is added dropwise at room temperature over the course of 5 min to this yellow-green solution. The mixture is brought to reflux for 20 h. The reaction mixture, which is violet in colour, is hydrolyzed by saturated aqueous ammonium chloride solution, then extracted with ethyl acetate. The organic phase is washed with saturated aqueous NaCl solution, then dried over MgSO4. The solvent is evaporated under reduced pressure. The desired product is purified by chromatography with an eluent: 9:1 hexane/ethyl acetate, and is obtained in the form of an oil (0.9 g; 36%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05543298 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-16d7511e36964d53a2fa087f584c47ec |
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| Source note | uspto-grants-1996_08 |
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