HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1,4,6-Tetramethyl-5,7-dinitro-2,3-dihydro-1H-indene → 3,3,5,7-Tetramethyl-2,3-dihydro-1H-indene-4,6-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1,4,6-Tetramethyl-5,7-dinitro-2,3-dihydro-1H-indene | HCID 18179341 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3,3,5,7-Tetramethyl-2,3-dihydro-1H-indene-4,6-diamine | HCID 18179318 | — |
Reaction Steps
One hundred seventy-five grams (0.662 mol) of the 5,7-dinitro-1,1,4,6-tetramethylindane thus obtained were dissolved in 500 g of methanol, and after addition of 17.5 g of 5% Pd/C (water content: 50%) to the resultant solution, the mixture was stirred at 50-60° C. for 84 hours in a hydrogen gas atmosphere. After completion of the reaction, the reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The thus-obtained residue was distilled under reduced pressure to obtain 5,7-diamino-1,1,4,6-tetramethylindane as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04987261 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-cdc653b5b842445fbcb0a1db009f923a |
| Source note | uspto-grants-1991_01 |