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Chemical Structure| 1446394-07-5 Chemical Structure| 1446394-07-5

Structure of 1446394-07-5

Chemical Structure| 1446394-07-5

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Product Details of [ 1446394-07-5 ]

CAS No. :1446394-07-5
Formula : C66H72Br12O12
M.W : 2016.12
SMILES Code : BrCCOC1=C(CC2=CC(OCCBr)=C(CC3=CC(OCCBr)=C(CC4=CC(OCCBr)=C(CC5=C(OCCBr)C=C(CC6=C(OCCBr)C=C(C7)C(OCCBr)=C6)C(OCCBr)=C5)C=C4OCCBr)C=C3OCCBr)C=C2OCCBr)C=C(OCCBr)C7=C1

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Application In Synthesis of [ 1446394-07-5 ]

* 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 [ 1446394-07-5 ]

[ 1446394-07-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 50-00-0 ]
  • [ 5471-84-1 ]
  • [ 1446394-07-5 ]
YieldReaction ConditionsOperation in experiment
25% With iron(III) chloride; at 45℃; for 72h; 5 (2g, 6.17mmol), paraformaldehyde (926mg, 30.85mmol) and FeCl3 (200mg, 1.24mmol) were added to CHCl3 (90mL), and the mixture was heated to 45C for 72h. The mixture was cooled down to room temperature and then washed with water three times, the organic phase was concentrated and subjected to column chromatography (SiO2; Petroleum ether/CH2Cl2/EA, 2:1:0.06). Finally, a white solid was obtained (520mg, 25%). 1H NMR (400MHz, CDCl3): δ 6.78 (s, 12H), 4.17 (t, 24H, J=5.8Hz), 3.87 (s, 12H), 3.56 (t, 24H, J=5.8Hz). 13C NMR (101MHz, CDCl3): δ 150.19, 128.53, 115.84, 77.37, 77.05, 76.73, 68.97, 30.66, 30.35.
  • 2
  • [ 110-88-3 ]
  • [ 5471-84-1 ]
  • [ 1446394-07-5 ]
YieldReaction ConditionsOperation in experiment
25% With boron trifluoride diethyl etherate; In chloroform; at 20℃; for 2h;Inert atmosphere; To a solution of compound 4 (2.90 g, 9.00 mmol) and metaformaldehyde (2.40 g, 27.00 mmol) in CHCl3 (150 mL) was added Boron trifluoride etherate (1.92 g, 13.5 mmol) under an argon-gas atmosphere. After stirring at room temperature for 2 h, hydrochloric acid solution (1 mol/L, 20 mL) was added to quenching the reaction, and the reaction mixture was then washed successively with saturated sodium bicarbonate solution (2 × 50 mL) and saturated brine (2 × 50 mL) and dried with Na2SO4. The solvent was removed and the residue was purified by silica gel chromatography (eluent: petroleum ether/ dichloromethane, 1:2) to afford a white solid (0.75 g, 25%). 1H NMR (400 MHz, CDCl3) δ (ppm): 6.78 (s, 12H), 4.16 (t, J = 5.8Hz, 24H), 3.87 (s, 12H), 3.55 (t, J = 5.8Hz, 24H). 13C NMR (100 MHz, CDCl3) δ (ppm): 150.2, 128.5, 115.8, 69.0, 30.6, 30.3.
  • 3
  • [ 50-00-0 ]
  • [ 5471-84-1 ]
  • [ 1307270-15-0 ]
  • [ 1446394-07-5 ]
 

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