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Chemical Structure| 98453-58-8 Chemical Structure| 98453-58-8

Structure of 98453-58-8

Chemical Structure| 98453-58-8

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Product Details of [ 98453-58-8 ]

CAS No. :98453-58-8
Formula : C12H15Br
M.W : 239.15
SMILES Code : CC1(C)CCCC2=C1C=C(Br)C=C2
MDL No. :MFCD22041879

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Application In Synthesis of [ 98453-58-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 98453-58-8 ]

[ 98453-58-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 98453-58-8 ]
  • [ 98453-60-2 ]
YieldReaction ConditionsOperation in experiment
79% With chromium(VI) oxide; tert.-butylhydroperoxide; In dichloromethane; at 20℃; for 8h; 6-Bromo-4, 4-dimethyl-3, 4-dihydro-2H-naphthalen-1-one (Compound 3) To a solution of 7-bromo-1, 1-dimethyl-1, 2,3, 4-tetrahydro-naphthalene (Compound 2, 1. 1 g, 4.62 mmol) in 10 mL of dichloromethane was added chromium (VI) oxide (72 mg, 0.46 mmol) and 5 mL of ter-butyl hydroperoxide solution (TBHP). After stirring at room temperature for 8 h, the mixture was diluted with water (20 mL), extracted with diethyl ether (3x 10 mL), washed with brine (1 x 10 mL), dried (MgS04) and concentrated at reduced pressure. Purification by flash chromatography (90: 10 hexane/ethyl acetate) yielded the title compound (920 mg, 79 percent yield) as a white solid: 1H NMR (CDC13, 300 MHz) 8 7.87 (d, J = 8. 1 Hz, 1H), 7.54 (d, J = 2.1 Hz, 1H), 7.42 (dd, J = 2.1, 8.1 Hz, 1H), 2.70 (dd, J = 6.3, 7.5 Hz, 2H), 2.01 (dd, J = 6.3, 7.5 Hz, 2H), 1.38 (s, 6H).
79% With chromium(VI) oxide; tert.-butylhydroperoxide; In dichloromethane; at 20℃; for 8h; To a solution of 7-bromo-1,1-dimethyl-1,2,3,4-tetrahydro-naphthalene (Compound 15, 1.1 g, 4.62 mmol) in 10 mL of dichloromethane was added chromium (VI) oxide (72 mg, 0.46 mmol) and 5 mL of tert-butyl hydroperoxide solution (TBHP). After stirring at room temperature for 8 h, the mixture was diluted with water (20 mL), extracted with diethyl ether (3*10 mL), washed with brine (1*10 mL), dried (MgSO4) and concentrated at reduced pressure. Purification by flash chromatography (90:10 hexane/ethyl acetate) yielded the title compound (920 mg, 79percent yield) as a white solid: 1H NMR (CDCl3, 300 MHz) delta 7.87 (d, J=8.1 Hz, 1H), 7.54 (d, J=2.1 Hz, 1H), 7.42 (dd, J=2.1, 8.1 Hz, 1H), 2.70 (dd, J=6.3, 7.5 Hz, 2H), 2.01 (dd, J=6.3, 7.5 Hz, 2H), 1.38 (s, 6H).
53% With chromium(VI) oxide; In water; acetic acid; for 15h; c. 6-BROMO-4, 4-DIMETHYL-3, 4-DIHYDRO-2H-NAPHTHALEN-1-ONE A solution of 8.1 g (81 mmol) of chromium trioxide in 74 ml of acetic acid and 3.9 ml of water is added slowly to 14.3 g (60 mmol) of 7-BROM-1, 1- dimethyl-1, 2,3, 4-TETRAHYDRONAPHTHALENE dissolved in 1.5 1 of acetic acid. The reaction medium is stirred for 15 hours, reduced to a volume of 500 ml by concentration, hydrolysed with ice, extracted with ethyl ether and neutralized with 35percent sodium hydroxide solution. The solid obtained is washed with heptane. A pink-white powder is obtained (8 g; 53percent).
 

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