Diethyl Ether → 5-bromo-2',3',5',6'-tetrahydrospiro[indene-1,4'-pyran]-3(2H)-one

Temperature

-25 °C

To a solution of 6-bromo-1-indanone (0.50 g, 2.35 mmol) in anhydrous THF (40 mL) under N2 atmosphere at −78° C. was added a solution of NHMDS (1 M in THF, 2.5 mL, 2.5 mmol) within 30 min, followed by TMSCl (0.281 g, 0.327 mL 2.59 mmol) after stirred 30 min. To this reaction mixture was added NHMDS (1 M in THF, 6.0 mL, 6.0 mmol) within 30 min at this temperature. The temperature was allowed to warm to −30 to −20° C., after stirred another 30 min, 2,2-eichlorodiethyl ether (336 mg, 0.275 mL, 2.35 mmol) was added. Then the reaction temperature was allowed to warm to room temperature without removing cooling bath, and stirred overnight. The reaction was quenched with saturated aqueous NH4Cl, and extracted with EA two times. The combined organic phases were washed with 1 M HCl, H2O, brine successively, and dried over anhydrous Na2SO4, and filtered, and concentrated to give black oil. It was purified by flash chromatography on silica gel yield 103 mg of the desired product. MS ESI+ve m/z 281 (M+H)+.

1. stirringafter stirred another 30 min
2. temperatureto warm to room temperature
3. customwithout removing
4. temperaturecooling bath
5. stirringstirred overnight
6. customThe reaction was quenched with saturated aqueous NH4Cl
7. extractionextracted with EA two times
8. washThe combined organic phases were washed with 1 M HCl, H2O, brine successively
9. dry with materialdried over anhydrous Na2SO4
10. filtrationfiltered
11. concentrationconcentrated
12. customto give black oil
13. customIt was purified by flash chromatography on silica gel yield 103 mg of the desired product

ORD record

ord-05e190c921bc44928f5ca9bdf724835b

Source dataset

uspto-grants-2014_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08633212B2