HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2-Dimethyl-1H-indene-1,3(2H)-dione → 3-Hydroxy-2,2-dimethyl-1-indanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2-Dimethyl-1H-indene-1,3(2H)-dione | HCID 599983 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Hydroxy-2,2-dimethyl-1-indanone | HCID 13023681 | — |
Reaction Steps
To a solution of 2,2-dimethyl-indan-1,3-dione (430 mg, 2.47 mmol), in ethanol (80 mL) at −30° C. is added a solution of NaBH4 (29 mg, 0.74 mmol) in ethanol (3 mL). After one h the reaction is quenched with saturated aqueous NH4Cl and the mixture is brought to room temperature. The reaction mixture is concentrated to approximately half of its original volume and then diluted with ethyl acetate and washed with water. The aqueous layer is then back-extracted twice with ethyl acetate. The organic layers are combined, dried with Na2SO4, filtered, and concentrated. The resulting residue is purified by silica gel flash chromatography (ethyl acetate-heptane, 0:1 to 1:6) to afford 3-hydroxy-2,2-dimethyl-indan-1-one; MS (ESI) m/z 177.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153674B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-6ac45984c92841d9be45888f6d202f24 |
| Source note | uspto-grants-2012_04 |