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Chemical Structure| 138433-00-8 Chemical Structure| 138433-00-8

Structure of 138433-00-8

Chemical Structure| 138433-00-8

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Product Details of [ 138433-00-8 ]

CAS No. :138433-00-8
Formula : C43H80O4
M.W : 661.09
SMILES Code : OCC1=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C1

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Application In Synthesis of [ 138433-00-8 ]

* 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 [ 138433-00-8 ]

[ 138433-00-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 138433-00-8 ]
  • [ 162709-84-4 ]
YieldReaction ConditionsOperation in experiment
95% With pyridine; thionyl chloride; In tetrahydrofuran; at 20℃; for 1.5h; A mixture of 23 (2.00 g, 3.03 mmol), THF (30 mL), pyridine (0.733 mL, 9.09 mmol) and thionyl chloride (0.456 mL, 6.06 mmol) was stirred at ambient temperature for 1.5 h. After filtration, solvent inthe filtrate was removed under reduced pressure to give 1.96 g (95 %) of 24 as brown oil
95% With thionyl chloride; In dichloromethane; at 20℃; for 3h; Next, the compound shown in Chemical formula C is chlorinated with SOCl 2,To obtain the compound shown in Chemical Formula D.In this case, CH 2 Cl 2 was used as a solvent,The reaction was carried out at room temperature for 3 hours. The yield was 95%.
92% With thionyl chloride; N,N-dimethyl-formamide; In dichloromethane; at 20℃; for 0.5h; A mixture of 3,4,5-tridodecyloxybenzyl alcohol (5.49 g, 8.30 mmol), thionyl chloride (0.844 mL, 11.6 mmol), and DMF (0.10 mL) was stirred in CH2Cl2 (55 mL) for 30 min at room temperature. Removal of the solvent and excess thionyl chloride under reduced pressure gave 7 (5.20 g, 92%) as a colorless solid. 1H NMR (270 MHz, CDCl3) δ 0.88 (t, J=6.6 Hz, 9H, CH3), 1.15-1.40 (m, 48H), 1.40-1.54 (m, 6H, -O(CH2)2CH2-), 1.73 (tt, J=7.2, 7.2 Hz, 2H, -OCH2CH2-), 1.79 (tt, J=7.2, 7.2 Hz, 4H, -OCH2CH2-), 3.94 (t, J=7.2 Hz, 2H, -OCH2-), 3.97 (t, J=7.2 Hz, 4H, -OCH2-), 4.51 (s, 2H, CH2Cl), 6.56 (s, 2H, ArH); 13C NMR (68 MHz, CDCl3) δ 14.1, 22.7, 26.08, 26.11, 29.35, 29.37, 29.39, 29.60, 29.63, 29.65, 29.69, 29.72, 29.74, 30.32, 31.92, 31.94, 47.0, 69.1, 73.4, 107.1, 132.3, 153.2.
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