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Chemical Structure| 22041-21-0 Chemical Structure| 22041-21-0

Structure of 22041-21-0

Chemical Structure| 22041-21-0

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Product Details of [ 22041-21-0 ]

CAS No. :22041-21-0
Formula : C8H15NO2
M.W : 157.21
SMILES Code : O=C(OC)CCN1CCCC1
MDL No. :MFCD01695467

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Application In Synthesis of [ 22041-21-0 ]

* 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 [ 22041-21-0 ]

[ 22041-21-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 22041-21-0 ]
  • [ 19748-66-4 ]
YieldReaction ConditionsOperation in experiment
65% With lithium aluminium tetrahydride; In tetrahydrofuran; at 20℃; for 2h; Under the condition of ice-salt bath, 300 mL tetrahydrofuran was added into a 500 mL three-necked flask, and then 8 g LiAlH4 was portionwise added with keeping the temperature not exceeding 0° C. The solution of 30 g compound 81 dissolved in 30 mL THF was dropwise added, and gas released violently. The system was naturally warmed to room temperature. After 2 hours, the reaction had completed by checking by TLC. 100 mL THF solution containing 12percent water was added, and gas released violently. Then 30 mL of 15percent NaOH solution was added, and gas released a little. The system was added with 40 mL water, and then extracted with 70 mL dichloromethane for three times. The organic phases were merged, washed with salt water, dried with anhydrous sodiumsulfate, and concentrated to dryness to give 16 g yellow solid, i.e. compounds 92, 65percent yield. 1H-NMR (400 MHz, CDCl3) (ppm) 1.70-1.79 (m, 6H), 2.56-2.59 (m, 4H), 2.72-2.75 (m, 2H), 3.81 (t, J=5.6, 2H).
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20℃; General procedure: The respective secondary amine (1.0 equiv.) and methyl acrylate (1.1 equiv.) were stirred neat. On completion, excess methyl acrylate was removed under reduced pressure. The unpurified products were dissolved in THF (0.2 M) and added slowly to a cooled suspension of LiAlH4 (3equiv.) in THF at 0 °C. After 15 min the reaction was warmed to rt and stirred until it was complete by TLC. The mixture was cooled to 0 °C and worked-up by carefully adding the following in sequence: for n grams of LiAlH4, water (n mL), 10percent NaOH (aq., n mL), and water (3 x n mL). After adding MgSO4, the aluminum salts were removed by filtration, and was hed portion-wise with ether. Removal of the solvent under reduced pressure provided the products as oils. Purification by flash column chromatography provided the amino alcohols.
 

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