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Chemical Structure| 5544-60-5 Chemical Structure| 5544-60-5

Structure of 5544-60-5

Chemical Structure| 5544-60-5

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Product Details of [ 5544-60-5 ]

CAS No. :5544-60-5
Formula : C14H13BrO
M.W : 277.16
SMILES Code : BrCC1=CC=C(OCC2=CC=CC=C2)C=C1
MDL No. :MFCD07368336
InChI Key :KHZAFUOYPXXJKO-UHFFFAOYSA-N
Pubchem ID :10492756

Safety of [ 5544-60-5 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P260-P264-P270-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P405-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 5544-60-5 ]

* 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 [ 5544-60-5 ]

[ 5544-60-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 5544-60-5 ]
  • [ 107819-90-9 ]
  • [ 641611-50-9 ]
  • 2
  • [ 5544-60-5 ]
  • [ 62327-21-3 ]
  • [ 1407507-27-0 ]
YieldReaction ConditionsOperation in experiment
20% yl]-2-{dimethoxyphosphoryl)propanoate; To a suspension of 1 .71 g sodium hydride (50 percent in oil, 35.7 mmol) in anhydrous tetrahydrofuran (100 mL) was added a solution of 8.0 g ierf-butyl P,P- dimethylphosphonoacetate (35.7 mmol) in anhydrous tetrahydrofuran (25 mL) at room temperature, and the resulting mixture was stirred for 1 h at room temperature. Subsequently, a solution of 4.95 g 4-benzyloxybenzyl bromide (17.8 mmol; prepared according to Helv. Chim. Acta, 2002, 85, 3422) in tetrahydrofuran (25 mL) was added, and the mixture was stirred at room temperature overnight. Saturated aqueous ammonium chloride (50 mL) was then added, the mixture was stirred for another 20 minutes at room temperature, and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate and evaporated. Column chromatography over silica gel (2.5 --> 50 percent ethyl acetate in hexane) gave 1 .48 g (20 percent yield based on 4- benzyloxybenzyl bromide) of the target compound. 1H-NMR (400 MHz, CHLOROFORM-d): delta [ppm]= 1 .34 (s, 9 H), 3.06 - 3.22 (m, 3 H), 3.81 (s br, 3 H), 3.83 (s br, 3 H), 5.05 (s, 2 H), 6.89 (d, 2 H), 7.13 (d, 2 H), 7.29 - 7.45 (m, 5 H).ESI+ m/z 365 (M+H-C4H8, m/z (M+H) 421 , m/z (M +NH4) 438.
20% To a suspension of 1.71 g sodium hydride (50 percent in oil, 35.7 mmol) in anhydrous tetrahydrofuran (100 mL) was added a solution of 8.0 g tert-butyl P,P-dimethylphosphonoacetate (35.7 mmol) in anhydrous tetrahydrofuran (25 mL) at room temperature, and the resulting mixture was stirred for 1 h at room temperature.Subsequently, a solution of 4.95 g 4-benzyloxybenzyl bromide (17.8 mmol; prepared according to ) in tetrahydrofuran (25 mL) was added, and the mixture was stirred at room temperature overnight.Saturated aqueous ammonium chloride (50 mL) was then added, the mixture was stirred for another 20 minutes at room temperature, and extracted with ethyl acetate.The organic layer was dried over magnesium sulfate and evaporated.Column chromatography over silica gel (2.5 ? 50 percent ethyl acetate in hexane) gave 1.48 g (20 percent yield based on 4-benzyloxybenzyl bromide) of the target compound.1H-NMR (400 MHz, CHLOROFORM-d): delta [ppm]= 1.34 (s, 9 H), 3.06 - 3.22 (m, 3 H), 3.81 (s br, 3 H), 3.83 (s br, 3 H), 5.05 (s, 2 H), 6.89 (d, 2 H), 7.13 (d, 2 H), 7.29 - 7.45 (m, 5 H).ESI+ m/z 365 (M+H-C4H8, m/z (M+H) 421, m/z (M +NH4) 438.
 

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