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Chemical Structure| 107017-72-1 Chemical Structure| 107017-72-1

Structure of 107017-72-1

Chemical Structure| 107017-72-1

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Product Details of [ 107017-72-1 ]

CAS No. :107017-72-1
Formula : C4H9NO
M.W : 87.12
SMILES Code : NC1(CC1)CO
MDL No. :MFCD01318221

Safety of [ 107017-72-1 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H314
Precautionary Statements:P280-P301+P330+P331-P305+P351+P338-P310
Class:6.1(8)
UN#:2928
Packing Group:

Application In Synthesis of [ 107017-72-1 ]

* 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 [ 107017-72-1 ]

[ 107017-72-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 42303-42-4 ]
  • [ 107017-72-1 ]
YieldReaction ConditionsOperation in experiment
98% Example 67; 5-Cvano-1-(3-trifluoromethoxybenzyl)-1H-indole-2-carboxylic acid (1- hvdroxymethylcvclopropyDamide1-Amino-cyclopropanecarboxylic acid ethyl ester hydrochloride (350mg, 2.11mmol) was dissolved in anhydrous THF (15ml) and cooled to 00C under argon. A 1.0M solution of lithium aluminium hydride in THF (2.5ml, 2.50mmol) was added dropwise and the reaction allowed to warm to room temperature and stirred for 17 h. The reaction was quenched by EPO <DP n="51"/>cautious addition of sodium sulfate decahydrate until evolution of hydrogen had ceased. The suspension was stirred for 2 h, filtered through Dicalite and the residue washed thoroughly with ether. The filtrate and washings were combined and concentrated to yield (i-amino-cyclopropyl)methanol (180mg, 98%) as a colourless oil.
95% With lithium aluminium tetrahydride; In tetrahydrofuran; at 0℃; for 2h;Inert atmosphere; To a stirred solution of lithium aluminum hydride (1.3 g, 36.23 mmol) in THF (30 mL) under an argon atmosphere was added <strong>[42303-42-4]ethyl 1-aminocyclopropane-1-carboxylate hydrochloride</strong> (3 g, 18.11 mmol) at 0 oC and stirred for 2 h. After consumption of starting material (monitored by TLC), the reaction mixture was quenched with a saturated sodium sulfate solution (100 mL) and stirred for 1 h. The reaction mixture was filtered and washed with 20% MeOH: CH2Cl2. The filtrate was concentrated in vacuo to obtain (1- aminocyclopropyl) methanol (1.5 g, 95%) as a colorless liquid used in the next step without further purification. TLC: EtOAc (Rf: 0.1).
 

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