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Chemical Structure| 193354-16-4 Chemical Structure| 193354-16-4

Structure of 193354-16-4

Chemical Structure| 193354-16-4

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Product Details of [ 193354-16-4 ]

CAS No. :193354-16-4
Formula : C9H10IN
M.W : 259.09
SMILES Code : IC1=CC2=C(NCCC2)C=C1
English Name :6-Iodo-1,2,3,4-tetrahydroquinoline
MDL No. :MFCD10699455

Safety of [ 193354-16-4 ]

Application In Synthesis of [ 193354-16-4 ]

* 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 [ 193354-16-4 ]

[ 193354-16-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 635-46-1 ]
  • [ 193354-16-4 ]
YieldReaction ConditionsOperation in experiment
50% With dihydrogen peroxide; iodine In water at 20℃; 9.A To a mixture of 1 ,2,3,4,- tetrahydroquinoline (0.34 g; 2.55 mmol) and I2 (0.32 g; 1.27 mmol) in H2O (10 ml), 30% H2O2 (0.26 ml; 2.55 mmol) was added at room temperature. The resulting mixture was vigorously stirred overnight at room temperature, and then extracted with Et2O (2 x 15 ml). The combined organic phase was washed with H2O, brine, dried over anhydrous MgSO4 and filtered. The filtrate was evaporated under reduced pressure and the residue was purified by FCC (SiO2; CH2CI2), to give the title compound (0.33 g; 50%) as a creamy syrup. 1 H-NMR (CDCI3) 1 .84 - 1 .92 (m, 2H); 2.69 (tr, 2H, J = 6.4 Hz); 3.27 (tr, 2H, J = 6.4 Hz); 3.82 (broad S, 1 H); 6.22 (d, 1 H, J = 8.2 Hz); 7.15 - 7.21 (m, 2H).
With iodine; sodium hydrogencarbonate In tetrahydrofuran; water at 20℃; 6-iodo-1,2,3,4-tetrahydroquinoline (1a) General procedure: NaHCO3 (1.11 mmol, 3.0 equiv) in water (10 mL) andiodine (0.55 mmol, 1.5 equiv) were added to a solutionof 1,2,3,4-tetrahydroquinoline I (0.37 mmol, 1.0 equiv)in tetrahydrofuran (6.5 mL) at 0 °C. The reaction mixturewas agitated at an ambient temperature for one night.Subsequently, it was extracted using dichloromethane inthree separate aliquots of 30 mL each. The organic layer,a combination of several substances, was washed usingsodium thiosulfate. It was then dehydrated using anhydrousNa2SO4, filtered, and condensed. The unrefined residueunderwent purification using column chromatographyusing hexane as the eluent, resulting in the production ofiodide THQ 1a as a yellowish oil (Yield 60%) comparableto those reported in the literature.The compound chromanone II (0.978 g, 6.60 mmol)was dissolved in acetic acid (5 mL) and added to a suspensionof zinc dust (10.8 g, 1.65 mol) in acetic acid (50 mL).The mixture was subjected to heating at a temperature of100 °C and agitated for a night. It then passed throughCelite, washed with 100 mL of ethyl acetate. The resultingsolution was diluted with 300 mL of phenylmethaneand subsequently concentrated, resulting in the formationof intermediate chromane III.Sequentially, 1.2 g (equivalent to 7.06 mmol) of AgNO3and 1.58 g (equivalent to 6.23 mmol) of I2were added toa mixture containing 0.845 g (equivalent to 6.3 mmol)of chromane III and 20 ml of MeOH. The mixture wasstirred for approximately 1 h and then passed through afilter containing Celite. The resulting liquid was thenconcentrated by reducing the pressure. The remainingsubstance was mixed with ethyl acetate (25 mL) and thenrinsed with a solution of saturated sodium thiosulfate (25mL). The aqueous layer was rinsed with 20 mL of water,dehydrated using Na2SO4,filtered, and then concentrated.The remaining substance was additionally refined usingflash column chromatography using silica gel and a mixtureof 5% ethyl acetate in hexanes, resulting in the formationof 6-iodochroman 1b (Yield 73% over 2 steps). Allspectroscopic and analytical properties were identical tothose reported in the literature
  • 2
  • [ 13327-31-6 ]
  • [ 193354-16-4 ]
YieldReaction ConditionsOperation in experiment
88% With trifluorormethanesulfonic acid; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate In dichloromethane; water at 20℃; for 2h; Sealed tube; chemoselective reaction;
87% With bis(cyclopentadienyl)titanium dichloride; ammonia borane; sodium methylate In tetrahydrofuran at 120℃; for 24h; Sealed tube; chemoselective reaction;
With hydrogen In toluene at 100℃; for 5h; Autoclave;
With hydrogen In isopropyl alcohol at 100℃; for 8h; Autoclave; Catalytic testing. General procedure: Hydrogenation was carried out in a stainless-steel autoclave equipped with a pressurecontrol system. Typically, 1 mmol of quinolines and 10 mg of various catalysts weremixed in 2 mL of isopropanol. The reactions were performed in an autoclave purgedwith 1 MPa of H2 at 80 oC. The products were analyzed by gas chromatography-massspectrometer (GC-MS) and GC with m-xylene as the internal standard.
With ammonia borane In ethanol; water at 60℃; for 2h;
With ammonia borane In ethanol; water at 20℃; for 2h;
With BH5N(1-)*H(1+) In ethanol; water at 20℃;

 

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