p-Toluenesulfonic acid → 1,2-Dimethyl-1H-indene

A 200 ml four-necked flask equipped with a reflux tube, a thermometer and a dropping funnel was thoroughly purged with nitrogen and dried. To the flask, methylmagnesium bromide (3.0 mol/l ether solution)(16.9 ml, 50.7 mmol) and dehydrated ether (50 ml) were introduced. To the flask, a solution of 2-methyl-1-indanes (3.70 g, 25.3 mmol)in dehydrate ether (20 ml) was dropwise added at room temperature with stirring. Then, the reaction mixture was stirred for 2 hours and poured into cold water. The resultant mixture was introduced into a separatory funnel to separate an organic phase. The aqueous phase was extracted by ether (100 ml×3) and a combined organic phase was washed with a saturated aqueous solution of ammonium chloride, water and a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was distilled off to obtain 1,2-dimethyl-1-hydroxy-indene. The compound thus obtained was dissolved in toluene (30 ml) and, thereto, 0.1 g of p-toluenesulphonic acid was added. The reaction mixture was refluxed for 3 hours to remove water. The organic phase thus obtained was introduced into a separatory funnel and washed with a saturated aqueous solution of ammonium chloride, water and a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. After removing a solvent, it was purified by column chromatography (developer: hexane) to obtain 2.70 g (GC 94%) of a pale yellow solution (yield: 74%).

1. customThe compound thus obtained
2. temperatureThe reaction mixture was refluxed for 3 hours
3. customto remove water
4. customThe organic phase thus obtained
5. additionwas introduced into a separatory funnel
6. washwashed with a saturated aqueous solution of ammonium chloride, water
7. dry with materiala saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate
8. customAfter removing a solvent, it
9. customwas purified by column chromatography (developer: hexane)

ORD record

ord-7d0630afa6924aa1a43337b9a4ae77b4

Source dataset

uspto-grants-1999_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06004897