Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690770Generated: October 31, 2026

2,2-Dimethyl-1H-indene-1,3(2H)-dione → 3-Hydroxy-2,2-dimethyl-1-indanone

https://huagongshe.com/reaction/1690770

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Dimethyl-1H-indene-1,3(2H)-dioneHCID 599983—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product3-Hydroxy-2,2-dimethyl-1-indanoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153674B2
Source datasetuspto-grants-2012_04
ORD IDord-6ac45984c92841d9be45888f6d202f24
Source noteuspto-grants-2012_04