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Chemical Structure| 57614-92-3 Chemical Structure| 57614-92-3

Structure of 4-(4-Piperidyl)-1-butanol
CAS No.: 57614-92-3

Chemical Structure| 57614-92-3

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Product Details of [ 57614-92-3 ]

CAS No. :57614-92-3
Formula : C9H19NO
M.W : 157.25
SMILES Code : OCCCCC1CCNCC1
MDL No. :MFCD02178381
InChI Key :YRKCHKQZWFMCPB-UHFFFAOYSA-N
Pubchem ID :2784668

Safety of [ 57614-92-3 ]

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

Application In Synthesis of [ 57614-92-3 ]

* 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 [ 57614-92-3 ]

[ 57614-92-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 57614-92-3 ]
  • [ 24424-99-5 ]
  • [ 142355-83-7 ]
YieldReaction ConditionsOperation in experiment
54.7% With triethylamine; In dichloromethane; at 0 - 20℃; for 3h; A solution of 4-(piperidin-4-yl)butan-1 -ol (5, 1 .57 g, 10 mmol) and triethylamine (1 .50 mL, 10.5 mmol) in CH2CI2 (30 mL) was cooled to 0 C. Di-fert-butyl dicarbonate (2.30 g, 10.5 mmol) in CH2CI2 (5 mL) was added dropwise. After the addition, the mixture was stirred at 20 C for 3 h (monitored by TLC). The mixture was then washed with water (30 mL) and the organic layer concentrated in vacuo. The residue was purified by FC (4/1 PE/EtOAc ) to give 6 (2.16g, 54.7 %, MW = 253.345) as yellow oil. 1H NMR (400 MHz, CDCI3): δ = 4.09 (d, 2H, J = 1 1 .9 Hz), 3.67 (t, 2H, J = 6.6 Hz), 2.68 (t, 2H, J = 12.0 Hz), 1 .70-1 .63 (m, 2H), 1 .61 -1 .54 (m, 2H), 1 .47 (s, 9H), 1 .44-1 .36 (m, 3H), 1 .31 - 1 .25 (m, 2H), 1 .09 (qd, 2H, J = 12.6 Hz, 4.5 Hz).
In dichloromethane; at 20℃; 4- (Piperidin-4-yl) butan-l-ol(2 g, 12.72 mmol) was dissolved in dichloromethane (70 mL), and di-tert-butyl dicarbonate (3 g) was added at room temperature. After 5 minutes, water was added to terminate the reaction, and the reaction was repeated several times using ethyl acetateThe organic layer was washed with water and saturated sodium chloride solution, dried over sodium sulfate, and then concentrated. The resulting filtrate was purified by chromatography to obtain the desired compound as a colorless liquid.
 

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