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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53279Generated: October 29, 2026

6-Amino-3,3-dimethylindan-1-one → 6-Hydroxy-3,3-dimethyl-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/reaction/53279

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Amino-3,3-dimethylindan-1-oneHCID 12441789—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventTetrafluoroboric acidHCID 28118—
Product6-Hydroxy-3,3-dimethyl-2,3-dihydro-1H-inden-1-oneHCID 1936589950.3%

Reaction Steps

A solution of sodium nitrite (14.8 g, 214 mmol) in 30 mL of water was slowly added to the solution of 6-amino-3,3-dimethyl-indan-1-one (14.0 g, 85.8 mmol) in 30 mL of 48% tetrafluoroboric acid and 30 mL of water at 0°-5° C. After being stirred for 30 min, the mixture was filtered, and the solids were washed with cold 5% tetrafluoroboric acid and dried in vacuum. The solids were then added in several portions into a boiling solution of 50 mL of sulfuric acid in 0.5 liter of water. After refluxing for 1 hour, the solution was cooled to room temperature and extracted with ethyl acetate (100 mL×3). The combined extracts were dried over magnesium sulfate and evaporated. The residue was purified by flash chromatography (EtOAc:hexane=1:10 to 1:2) to give 7.60 g (50% yield) of the title compound as a solid; 1H-NMR (CDCl3) δ1.40 (s, 6H), 2.64 (s, 2H), 7.13 (s, 1H),7.18 (d, J=8.2 Hz, 1H), 7.39 (d, J=8.2 Hz, 1H); MS m/e 177 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618839
Source datasetuspto-grants-1997_04
ORD IDord-d863d2c7169d4eaa9fad627b62a0ac69
Source noteuspto-grants-1997_04