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[ CAS No. 14446-29-8 ] {[proInfo.proName]}

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Chemical Structure| 14446-29-8
Chemical Structure| 14446-29-8
Structure of 14446-29-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 14446-29-8 ]

CAS No. :14446-29-8 MDL No. :N/A
Formula : C10H11NO Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 161.20 Pubchem ID :-
Synonyms :

Safety of [ 14446-29-8 ]

Signal Word: Class:N/A
Precautionary Statements: UN#:N/A
Hazard Statements: Packing Group:N/A

Application In Synthesis of [ 14446-29-8 ]

* 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.

  • Upstream synthesis route of [ 14446-29-8 ]
  • Downstream synthetic route of [ 14446-29-8 ]

[ 14446-29-8 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 42923-77-3 ]
  • [ 52986-70-6 ]
  • [ 14446-29-8 ]
Reference: [1] Advanced Synthesis and Catalysis, 2017, vol. 359, # 14, p. 2358 - 2363
  • 2
  • [ 14446-29-8 ]
  • [ 42923-77-3 ]
YieldReaction ConditionsOperation in experiment
76% With sodium borohydrid In methanol; dichloromethane; water Referential Example 137
6-Methoxy-1,2,3,4-tetrahydroisoquinoline
In methanol (100 ml), 6-methoxy-3,4-dihydroisoquinoline (10.4 g) was dissolved.
After the addition of water (10 ml) and then sodium borohydride (6.10 g), the resulting mixture was stirred at room temperature for 15 minutes.
The reaction mixture was concentrated under reduced pressure and the residue was dissolved in dichloromethane.
The resulting solution was washed with water.
The organic layer so separated was dried over anhydrous sodium sulfate.
The solvent was then distilled off under reduced pressure.
The residue was purified by chromatography on a silica gel column (dichloromethane~dichloromethane:methanol=100:15), whereby the title compound (7.95 g, 76percent) was obtained.
1H-NMR (CDCl3) δ: 2.79(2H,t,J=5.9 Hz), 3.12(2H,t,J=5.9 Hz), 3.76(3H,s), 3.96(2H,s), 6.62(1H,s), 6.70(1H,dd,J=8.3,2.4 Hz), 6.92(1H,d,J=8.3 Hz).
MS (FAB) m/z: 164 (M+H)+.
Reference: [1] Patent: US6525042, 2003, B1,
  • 3
  • [ 110339-54-3 ]
  • [ 14446-29-8 ]
  • [ 2039-67-0 ]
Reference: [1] Journal of Chemical Research, Miniprint, 1987, # 2, p. 501 - 526
  • 4
  • [ 14446-29-8 ]
  • [ 57196-62-0 ]
Reference: [1] Journal of Chemical Research, Miniprint, 1987, # 2, p. 501 - 526
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