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Chemical Structure| 1458652-81-7 Chemical Structure| 1458652-81-7

Structure of 1458652-81-7

Chemical Structure| 1458652-81-7

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Product Details of [ 1458652-81-7 ]

CAS No. :1458652-81-7
Formula : C13H19BrO2
M.W : 287.19
SMILES Code : OCC(C)(C)COC1=CC(C)=C(Br)C(C)=C1
MDL No. :MFCD31628808

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Application In Synthesis of [ 1458652-81-7 ]

* 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 [ 1458652-81-7 ]

[ 1458652-81-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1003-85-6 ]
  • [ 7463-51-6 ]
  • [ 1458652-81-7 ]
YieldReaction ConditionsOperation in experiment
251 mg With caesium carbonate; In N,N-dimethyl-formamide; at 100℃; for 12.0h; Step 2: 3-(4-Bromo-3,5-dimethylphenoxy)-2,2-dimethylpropan-1-ol To a mixture of 4-bromo-3,5-dimethylphenol (625 mg) and Cs2CO3 (5 g) in N,N-dimethylformamide (10 mL) is added 5,5-dimethyl-[1,3,2]dioxathiane-2-oxide (467 mg). The mixture is stirred for 12 hours at 100 C. and then partitioned between water and ethyl acetate. The organic phase is washed with brine and dried (MgSO4). The solvent is evaporated and the residue is purified by HPLC on reversed phase to give the title compound. Yield: 251 mg; LC (method 7): tR=1.16 min; Mass spectrum (ESI+): m/z=287 [M+H]+.
372 mg With caesium carbonate; In N,N-dimethyl-formamide; at 120℃; for 12.0h;Microwave irradiation; Sealed tube; I n a m icrowave vial CS2CO3 (5.4 g) is added to a soltuion of 5,5-dimethyl- [1 ,3,2]dioxathiane 2-oxide (500 mg) and 4-bromo-3,5-dimethylphenol (670 mg) in Ν,Ν-dimethylformamide (5 mL). The vial is sealed and the mixture is heated to 120C for 12 hours. The mixture is partitioned between ethyl acetate and water. The organic phase is washed three times with 2 M aqueous NaOH and with brine. After drying (MgSO4) and concentration the residue is chromatographed on silica gel (cyclohexane/ethyl acetate 99:1→50:50) to give the title compound. Yield: 372 mg; LC (method 7): tR = 1 .17 min; Mass spectrum (ESI+): m/z = 287 [M+H]+.
372 mg With caesium carbonate; In N,N-dimethyl-formamide; at 120℃; for 12.0h;Microwave irradiation; Sealed tube; I n a m icrowave vial CS2CO3 (5.4 g) is added to a soltuion of 5,5-dimethyl- [1 ,3,2]dioxathiane 2-oxide (500 mg) and 4-bromo-3,5-dimethylphenol (670 mg) in N,N-dimethylformamide (5 mL). The vial is sealed and the mixture is heated to 120C for 12 hours. The mixture is partitioned between ethyl acetate and water. The organic phase is washed three times with 2 M aqueous NaOH and with brine. After drying (MgSO4) and concentration the residue is chromatographed on silica gel (cyclohexane/ethyl acetate 99:1→50:50) to give the title compound. Yield: 372 mg; LC (method 7): tR = 1 .17 min; Mass spectrum (ESI+): m/z = 287 [M+H]+.
 

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