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Chemical Structure| 62957-60-2 Chemical Structure| 62957-60-2

Structure of 62957-60-2

Chemical Structure| 62957-60-2

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Product Details of [ 62957-60-2 ]

CAS No. :62957-60-2
Formula : C4H7NO
M.W : 85.10
SMILES Code : N#CCOCC
MDL No. :MFCD09934087

Safety of [ 62957-60-2 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H302+H312+H332
Precautionary Statements:P210-P233-P240-P241+P242+P243-P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312+P362+P364-P304+P340+P312-P370+P378-P403+P235-P501
Class:3
UN#:1993
Packing Group:

Application In Synthesis of [ 62957-60-2 ]

* 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 [ 62957-60-2 ]

[ 62957-60-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 62957-60-2 ]
  • [ 2734-70-5 ]
  • N-(2,6-dimethoxyphenyl)-2-ethoxyacetimidamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
57% With trimethylaluminum; In toluene; at 110℃; for 14h;Cooling with ice; Trimethylaluminum (2 M in toluene, 4.70 ml, 9.40 mmol) was added dropwise to a solution of <strong>[2734-70-5]2,6-dimethoxyaniline</strong> (1.2 g, 7.8 mmol) and Compound 3b (0.80 g, 9.4 mmol) in toluene (10 ml) while cooling in an ice bath. After addition was complete, the reaction mixture was heated to 110 C. and was stirred at this temperature for 14 h. The reaction mixture was allowed to cool and was partitioned between a saturated solution of Rochelle's salt and EtOAc. The organic phase was separated, dried over MgSO4, filtered and concentrated under reduced pressure. The residue was added to a silica gel (120 g) column and was eluted with 0-20% of 20% MeOH/DCM in 0.5% TEA/DCM to give Compound 3c (1.1 g, 57%) as a brown liquid. MS m/z=239.0 (M+H). 1H NMR (500 MHz, CDCl3) δ 7.01 (t, J=8.3 Hz, 1H), 6.62 (d, J=7.7 Hz, 2H), 5.32 (s, 2H), 4.88 (br s, 2H), 4.31 (s, 2H), 3.82 (s, 6H), 3.62-3.73 (m, 2H), 1.19-1.33 (m, 3H).
57% With trimethylaluminum; In toluene; at 110℃; for 14h;Cooling with ice; Trimethylalurninum (4.7 mL, 9.4 mmol) was added dropwise to a solution of <strong>[2734-70-5]2,6-dimethoxyaniline</strong> (1.2 g, 7.8 mmol) and Compound lb (0.80 g, 9.4 mmol) in toluene (10mL) while cooling in an ice bath. After addition was complete, the reaction mixture was warmed to 110 C and was stirred at this temperature for l4hrs. The cooled reaction mixture was partitioned between a saturated solution of Rochelle’s salt and EtOAc. The organic phase was separated, dried over MgSO4, filtered and concentrated under reducedpressure. The resulting residue was added to a silica gel (120 g) colunm and was eluted with 0-20% of 20% MeOH/DCM in 0.5% TEA/DCM to give Compound lc (1.1 g, 4.5 mmol, 57 %) as a brown liquid. MS ,n/z 239.0 (M+H). 1H NMR (500M1-lz, CDC13) 67.01(t, J 8.3 Hz, 1H), 6,62 (d, J= 7.7 Hz, 2H), 5.32 (s, 2H), 4.88 (hr s, 2H), 4.31 (s,2H), 3.82 (s, 6H), 3.62-3.73 (m, 2H), 1.19-1.33 (m, 3H).
 

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