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Chemical Structure| 124854-96-2 Chemical Structure| 124854-96-2

Structure of 124854-96-2

Chemical Structure| 124854-96-2

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Product Details of [ 124854-96-2 ]

CAS No. :124854-96-2
Formula : C17H15BrO2
M.W : 331.20
SMILES Code : OC(C=C1CCOC1=C2)=C2C/C=C/C3=C(Br)C=CC=C3
MDL No. :N/A

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Application In Synthesis of [ 124854-96-2 ]

* 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 [ 124854-96-2 ]

[ 124854-96-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 40492-52-2 ]
  • [ 124854-95-1 ]
  • [ 124854-96-2 ]
YieldReaction ConditionsOperation in experiment
1.58 g (40%) In hexane; ethyl acetate; mineral oil; benzene; Step C: Preparation of 6-(o-bromocinnamyl)-2,3-dihydro-5-hydroxybenzofuran Sodium hydride (0.72 g; 18 mM, 60% in mineral oil) was washed twice with hexane under a stream of nitrogen. It was then suspended in 25 ml of anhydrous benzene in a 250 ml side-arm round bottom flask equipped with a dropping funnel. The <strong>[40492-52-2]5-hydroxy-2,3-dihydrobenzofuran</strong> was added in one portion (1.63 g; 12.0 mM) in 40 ml of benzene under positive nitrogen pressure and the resulting suspension was stirred at room temperature for 45 minutes. o-Bromocinnamyl bromide was then added in 15 ml of benzene. No reaction was observed at R.T. or at 50 so the reaction was heated to 75 for two hours at which time the reaction was cooled to 23 and poured into dilute hydrochloric acid solution. This was extracted 3 times with ether, dried over magnesium sulfate, and stripped to a brown oil. This crude material was purified by chromatography on a Waters' Prep 500 equipped with one cartridge and eluted and recycled with 20% ethyl acetate in hexane. Recrystallization from ethyl acetate/hexane gave 1.58 g (40%) of tan crystals identified spectrally as 6-(o-bromocinnamyl)-2,3-dihydro-5-hydroxybenzofuran. MNR (CDCl3): delta6.6-7.4 (m; 4H); 6.4-6.6 (m; 3H); 6.08 (dqt (16 Hz & 6 Hz); 1H); 4.67 (s; 1H); 4.40 (t(8 Hz); 2H); 3.43 (d(6 Hz); 2H); 3.03 (t(8 Hz); 2H). IR: 3700, 3500, 2950, 1480, 1430, 1330, 1280, 1160, 1140, 1020, 980, 965, 945, 865 cm-1 (CHCl3).
1.58 g (40%) In hexane; ethyl acetate; mineral oil; benzene; Step C: Preparation of 6-(o-bromocinnamyl)-2,3-dihydro-5-hydroxybenzofuran Sodium hydride (0.72 g; 18 mM, 60% in mineral oil) was washed twice with hexane under a stream of nitrogen. It was then suspended in 25 ml of anhydrous benzene in a 250 ml side-arm round bottom flask equipped with a dropping funnel. The <strong>[40492-52-2]5-hydroxy-2,3-dihydrobenzofuran</strong> was added in one portion (1.63 g; 12.0 mM) in 40 ml of benzene under positive nitrogen pressure and the resulting suspension was stirred at room temperature for 45 minutes. o-Bromocinnamyl bromide was then added in 15 ml of benzene. No reaction was observed at R.T. or at 50 so the reaction was heated to 75 for two hours at which time the reaction was cooled to 23 and poured into dilute hydrochloric acid solution. This was extracted 3 times with ether, dried over magnesium sulfate, and stripped to a brown oil. This crude material was purified by chromatography on a Waters' Prep 500 equipped with one cartridge and eluted and recycled with 20% ethyl acetate in hexane. Recrystallization from ethyl acetate/hexane gave 1.58 g (40%) of tan crystals identified spectrally as 6-(o-bromocinnamyl)-2,3-dihydro-5-hydroxybenzofuran. NMR (CDCl3): delta6.6-7.4 (m; 4H); 6.4-6.6 (m; 3H); 6.08 (dqt (16 Hz & 6 Hz); 1H); 4.67 (s; 1H); 4.40 (t(8 Hz); 2H); 3.43 (d(6 Hz); 2H); 3.03 (t(8 Hz); 2H). IR: 3700, 3500, 2950, 1480, 1430, 1330, 1280, 1160, 1140, 1020, 980, 965, 945, 865 cm-1 (CHCl3)
  • 2
  • [ 40492-52-2 ]
  • [ 124854-96-2 ]
 

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