HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-hydroxy-2,3-dihydro-1H-indene-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Oxo-2,3-Dihydro-1H-Indene-4-Carbonitrile | HCID 2751583 | — |
| Reactant | Potassium borohydride | HCID 4192641 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-hydroxy-2,3-dihydro-1H-indene-4-carbonitrile | HCID 14515307 | 94.7% |
Reaction Steps
1.46 g of 4-cyano-1-indanone in 131 ml of tetrahydrofuran is cooled to +5° C., 1 g of potassium borohydride is added in small fractions, with agitation for one hour 15 minutes, followed by pouring over 200 ml of water containing sodium chloride, and extraction with isopropyl ether. The organic phase is dried, brought to dryness under reduced pressure and the residue is chromatographed on silica in a hexane-ethyl acetate mixture (6-4). 1.40 g of expected product is obtained, M.p.=98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05180741 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-3d6a303bbf2a4ede8595cd26d21fe8b9 |
| Source note | uspto-grants-1993_01 |