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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089484Generated: October 30, 2026

2,2-dimethyl-2,3-dihydro-1H-inden-1-one → 2,3-Dihydro-2,2-dimethyl-1H-inden-1-ol

https://huagongshe.com/reaction/2089484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-dimethyl-2,3-dihydro-1H-inden-1-oneHCID 301202—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product2,3-Dihydro-2,2-dimethyl-1H-inden-1-olHCID 10942771—

Reaction Steps

To a solution of 2,2-dimethyl-indan-1-one, which can be prepared as described in Ranu, B. C.; Jana, U. Journal of Organic Chemistry, 1999, 64, 6380-6386, (13.0 g, 81.3 mmol) in methanol (200 mL) at −20° C. is added NaBH4 (3.07 g, 81.3 mmol). Upon complete consumption of the starting ketone, as determined by TLC analysis, the reaction is quenched with saturated aqueous NH4Cl. The reaction mixture is then concentrated to near dryness, diluted with ethyl acetate and washed with water. The organic layer is then dried with Na2SO4, filtered, and concentrated. The resulting residue is purified by silica gel flash chromatography (ethyl acetate-heptane, 0:1 to 1:8) to provide 2,2-dimethyl-indan-1-ol. 1H NMR (400 MHz, CDCl3) δ ppm 1δ ppm 1.05 (s, 3 H), 1.20 (s, 3 H), 2.56-2.89 (m, 2 H), 4.70 (s, 1 H), 7.16-7.26 (m, 3 H), 7.35-7.42 (m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436035B2
Source datasetuspto-grants-2013_05
ORD IDord-43cdb17aa4ae4eb099ebf12d79faed40
Source noteuspto-grants-2013_05