HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → 5,6-Dichloro-indan-1-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 5,6-Dichloro-2,3-dihydro-1H-inden-1-one | HCID 22903609 | — |
| Product | 5,6-Dichloro-indan-1-ylamine | HCID 20323400 | — |
Reaction Steps
Following the procedure of Example 1, 5,6-dichloro-1-indanone was reacted with ammonium acetate and sodium cyanoborohydride to yield 5,6-dichloro-1-aminoindane; yield = 670 mg. The crystalline compound was treated with 360 mg. of maleic acid in 25 ml. of isopropanol. The maleate salt crystallized and was separated by filtration. Recrystallization of the salt from a 1:3 isopropanol/ethyl acetate solvent mixture yielded 650 mg. of 5,6-dichloro-1-aminoindane maleate melting at 167°-170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04096173 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-ff672ca82f8f47aca19d173fbfa32228 |
| Source note | uspto-grants-1978_06 |