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Product Details of [ 24211-54-9 ]

CAS No. :24211-54-9 MDL No. :MFCD06202374
Formula : C5H9NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :GPRZVNYVEZZOKH-BYPYZUCNSA-N
M.W : 115.13 Pubchem ID :10964456
Synonyms :

Safety of [ 24211-54-9 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 24211-54-9 ]

* 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 [ 24211-54-9 ]
  • Downstream synthetic route of [ 24211-54-9 ]

[ 24211-54-9 ] Synthesis Path-Upstream   1~10

  • 1
  • [ 24211-54-9 ]
  • [ 154307-84-3 ]
Reference: [1] Tetrahedron Asymmetry, 1993, vol. 4, # 9, p. 2085 - 2094
  • 2
  • [ 24211-53-8 ]
  • [ 24211-54-9 ]
YieldReaction ConditionsOperation in experiment
98% With 20% palladium hydroxide-activated charcoal; hydrogen In methanol at 25℃; for 24 h; To a solution of azide 13 (1.5 g, 10.62 mmol) in dry MeOH was added 20percent Pd(OH)2 (0.037 g, 0.53 mmol) and the reaction mixture was stirred under an atmosphere of H2 (1 atm) for 24 h at 25 oC. After completion of the reaction (monitored by TLC), the catalyst was filtered over Celite and the filtrate concentrated under reduced pressure to provide crude hydroxylactam, which was purified by column chromatography using ethyl acetate:methanol (9:1) as eluent to obtain pure hydroxylactam 14 (1.19 g, 98percent).
Reference: [1] Synthetic Communications, 2015, vol. 45, # 13, p. 1559 - 1565
[2] Tetrahedron, 1995, vol. 51, # 21, p. 5935 - 5950
[3] Tetrahedron Letters, 2005, vol. 46, # 8, p. 1247 - 1249
[4] Synthesis, 1986, vol. NO. 3, p. 232 - 233
[5] Journal of Organic Chemistry, 1985, vol. 50, # 6, p. 896 - 899
[6] Tetrahedron Asymmetry, 1996, vol. 7, # 6, p. 1811 - 1818
  • 3
  • [ 1179999-39-3 ]
  • [ 24211-54-9 ]
Reference: [1] Organic Letters, 2009, vol. 11, # 20, p. 4724 - 4727
  • 4
  • [ 32780-06-6 ]
  • [ 24211-54-9 ]
Reference: [1] Journal of Organic Chemistry, 1985, vol. 50, # 6, p. 896 - 899
[2] Synthesis, 1986, vol. NO. 3, p. 232 - 233
[3] Synthetic Communications, 2015, vol. 45, # 13, p. 1559 - 1565
  • 5
  • [ 58879-34-8 ]
  • [ 24211-54-9 ]
Reference: [1] Tetrahedron Asymmetry, 1996, vol. 7, # 6, p. 1811 - 1818
[2] Journal of Organic Chemistry, 1985, vol. 50, # 6, p. 896 - 899
  • 6
  • [ 102774-93-6 ]
  • [ 24211-54-9 ]
Reference: [1] Synthesis, 1986, vol. NO. 3, p. 232 - 233
[2] Synthetic Communications, 2015, vol. 45, # 13, p. 1559 - 1565
  • 7
  • [ 58960-19-3 ]
  • [ 24211-54-9 ]
  • [ 102774-92-5 ]
Reference: [1] Helvetica Chimica Acta, 2014, vol. 97, # 11, p. 1507 - 1515
  • 8
  • [ 591-80-0 ]
  • [ 24211-54-9 ]
Reference: [1] Synthetic Communications, 2015, vol. 45, # 13, p. 1559 - 1565
  • 9
  • [ 1729-32-4 ]
  • [ 24211-54-9 ]
Reference: [1] Synthetic Communications, 2015, vol. 45, # 13, p. 1559 - 1565
  • 10
  • [ 76543-09-4 ]
  • [ 24211-54-9 ]
Reference: [1] Synthetic Communications, 2015, vol. 45, # 13, p. 1559 - 1565
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