HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 67596793, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Amino-2,3-dihydro-1H-inden-1-one | HCID 414531 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 86754188 | HCID 86754188 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67596793 | HCID 67596793 | — |
Reaction Steps
2-Amino-6-chloro-1-indanone hydrochloride is prepared in the same way as in Example 1 for the preparation of 2-amino-1-indanone, starting from 57.5 g of 6-chloro-1-indanone oxime p-toluenesulphonate, 3.94 g of sodium, 200 ml of absolute ethanol and 1 litre of anhydrous toluene. After 15 hours of reaction at 0° C., the precipitate formed is filtered off on Celite, the filtrate washed with water and then extracted with IN hydrochloric acid (2×500 ml) and the aqueous phase concentrated to dryness under reduced pressure. 10.5 g of expected product are obtained in the form of a brown-green solid, the melting point of which is above 260° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05922716 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-24925a6c0e5649589f0df39f7b2822c1 |
| Source note | uspto-grants-1999_07 |