HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indene → 4-(1H-Inden-2-yl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indene | HCID 7219 | — |
| Reactant | 4-Iodoaniline | HCID 10893 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-(1H-Inden-2-yl)aniline | HCID 21714955 | — |
Reaction Steps
20 ml of triethylamine, 2.2 g (20 mmol) of indene, 4.38 g (20 mmol) of para-amino-iodo-benzene and 0.134 g (0.6 mmol) of Pd(OAc)2 were stirred under reflux for 10 h. After that all triethylamine was removed under reduced pressure. The residue was treated with 80 ml of 15% HCl. Forming precipitate was separated and washed with dichloromethane. The resulting substance was treated with the mixture 50 ml of dichloromethane and 50 ml of 5% KOH in water. Organic layer was separated, washed twice with water, filtered and dried over Na2SO4. Dichloromethane was removed and the residue was recrystallized from 20 ml of EtOH. The yield of product was 21%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06271411B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-c008d2c1833d47bba2fa66c6096c6460 |
| Source note | uspto-grants-2001_08 |