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Chemical Structure| 10282-30-1 Chemical Structure| 10282-30-1

Structure of 10282-30-1

Chemical Structure| 10282-30-1

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Product Details of [ 10282-30-1 ]

CAS No. :10282-30-1
Formula : C11H12N2
M.W : 172.23
SMILES Code : N1(CCCC1)C2=CC=C(C#N)C=C2
MDL No. :MFCD07368512
InChI Key :ZNMSYUCZLWETII-UHFFFAOYSA-N
Pubchem ID :4961271

Safety of [ 10282-30-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of [ 10282-30-1 ]

* 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 [ 10282-30-1 ]

[ 10282-30-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 10282-30-1 ]
  • [ 114365-04-7 ]
YieldReaction ConditionsOperation in experiment
86% With lithium aluminium tetrahydride; In diethyl ether; at 0 - 20℃; Benzonitrile 181 (1.68 g, 9.76 mmol) dissolved in 10 ml of ether was added drop wise at 0C to LiAlH4 (2equiv., 742 mg) suspended in diethyl ether (40 ml). The mixture was stirred at room temperature for 24 hours. The reaction was quenched by addition of water and filtrated and the salts were washed with ether. The organic phase was separated, anhydrified and evaporated giving 1.48 g of a yellow oil. Yield = 86% 'HNMR (DMSO, 200 MHz) δ 1.60 (2H, bs), 1.93 (4H, m), 3.17 (4H, m), 3.57 (2H, s), 6.46 (2H, d, J = 8.6 Hz), 7.09 (2H, d, J = 8.4 Hz).
86% With lithium aluminium tetrahydride; In diethyl ether; at 0 - 20℃; for 24h; Preparation of (4-(pyrrolidin-1-yl)phenyl)methanamine 21 Benzonitrile 181 (1.68 g, 9.76 mmol) dissolved in 10 ml of ether was added drop wise at 0C to LiA1H4 (2equiv., 742 mg) suspended in diethyl ether (40 ml). The mixture was stirred at room temperature for 24 hours. The reaction was quenched by addition of water and filtrated and the salts were washed with ether. The organic phase was separated, anhydrified and evaporated giving 1.48 g of a yellow oil. Yield = 86% 1HNMR (DMSO, 200 MHz) δ 1.60 (2H, bs), 1.93 (4H, m), 3.17 (4H, m), 3.57 (2H, s), 6.46 (2H, d, J = 8.6 Hz), 7.09 (2H, d, J = 8.4 Hz).
 

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