HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Indanone → HCID 15078222, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Indanone | HCID 11983 | — |
| Reactant | 4-Benzyloxyaniline hydrochloride | HCID 2723831 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15078222 | HCID 15078222 | 95% |
Reaction Steps
A solution of 1.00 g (4.2 mmol, Aldrich) of 4-benzyloxyaniline hydrochloride, 555 mg (4.20 mmol, Aldrich) of 2-indanone and 132 mg (2.10 mmol) of sodium cyanoborohydride in 25 ml of MeOH was stirred over 3A molecular sieves at 25° C. for one hour. The mixture was filtered, EtOAc was added and this was washed with saturated NaHCO3, dried (MgSO4) and concentrated in vacuo. Purification via flash chromatography (silica gel, 1:5 EtOAc/petroleum ether) afforded 1.25 g (95%) of title compound as a tan solid: m.p. 72°-75° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04975461 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-1d752ce6bcbc4a219490cde1b4e3a053 |
| Source note | uspto-grants-1990_12 |