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Chemical Structure| 5878-19-3 Chemical Structure| 5878-19-3

Structure of 5878-19-3

Chemical Structure| 5878-19-3

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Product Details of [ 5878-19-3 ]

CAS No. :5878-19-3
Formula : C4H8O2
M.W : 88.11
SMILES Code : CC(COC)=O
MDL No. :MFCD00008768
InChI Key :CUZLJOLBIRPEFB-UHFFFAOYSA-N
Pubchem ID :22172

Safety of [ 5878-19-3 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225
Precautionary Statements:P210-P403+P235
Class:3
UN#:1224
Packing Group:

Application In Synthesis of [ 5878-19-3 ]

* 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 [ 5878-19-3 ]

[ 5878-19-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 20265-35-4 ]
  • [ 5878-19-3 ]
  • [ 112777-36-3 ]
  • 2
  • [ 5878-19-3 ]
  • [ 100063-22-7 ]
  • [ 1007171-29-0 ]
YieldReaction ConditionsOperation in experiment
To a solution of methyl S-amino-δ-phenyl^-thiophenecarboxylate (2.0 g; 8.58 mmol) and acetic acid (5 ml.) in dry dichloromethane (100 ml.) was added methoxyacetone (0.91 g; 10.3 mmol) and the reaction mixture stirred at room temperature under nitrogen for 10 minutes. Sodium triacetoxyborohydride (3.6 g; 17.2 mmol) was added in 3 portions and the reaction mixture warmed to reflux under nitrogen for 3 days. A further equivalent sodium triacetoxyborohydride (1.8 g; 8.6 mmol) was added and the reaction mixture stirred to reflux under nitrogen for 2 days. Sodium bicarbonate solution (100 ml.) was added and the mixture stirred for 30 minutes, passed through a hydrophobic frit and evaporated to dryness. The crude product was purified by 120 g silica ISCO chromatography eluted with 0 - 100%EtOAc in cyclohexane to give the title compound.MS calcd for (Ci6H19NO3S + H)+: 306MS found (electrospray): (M+H)+ = 306
Intermediate 31Methyl 3-[1 -methyl-2-(methyloxy)ethyl]amino}-5-phenyl-2-thiophenecarboxylateTo a solution of methyl S-amino-δ-phenyl^-thiophenecarboxylate (2.0 g; 8.58 mmol) and glacial acetic acid (5 ml.) in dry dichloromethane (100 ml.) was added methoxyacetone (0.91 g, 10.3 mmol) and the reaction stirred at room temperature under nitrogen for 10 minutes. Sodium triacetoxyborohydride (3.6 g, 17.2 mmol) was added and the reaction heated at reflux under nitrogen for 3 days. A further addition of sodium triacetoxyborohydride (1.8 g, 8.6 mmol) was added and the reaction heated at reflux under nitrogen for 2 days. After <n="44"/>cooling to room temperature sodium bicarbonate solution (100 ml.) was added and the reaction stirred for 30 minutes, dried using a hydrophobic frit and evaporated to dryness. The crude product was purified by 120 g Si ISCO chromatography eluted EtOAc in cyclohexane (gradient from 0-100%) to give title compound. MS calcd for (Ci6H19NO3S + H)+: 306 MS found (electrospray): (M+H)+ = 306
  • 3
  • [ 942589-45-9 ]
  • [ 5878-19-3 ]
  • [ 1019338-38-5 ]
YieldReaction ConditionsOperation in experiment
A solution of methyl S-amino-delta-iodo^-thiophenecarboxylate (0.60 g, a synthesis of which is described as Intermediate 43), methoxyacetone (0.39 ml.) and titanium (IV) isopropoxide (0.74 ml.) in dry DCM (30 ml.) was warmed to reflux under nitrogen for 18 h. Sodium triacetoxyborohydride (1.35 g) was added and the reaction was heated at reflux under nitrogen for 4 days. The reaction was evaporated in vacuo and the residue was taken into water (30 ml.) and was extracted with DCM (3 x 30 ml_). The organics were dried by passing through a hydrophobic frit and evaporated in vacuo. The crude material was purified by <n="58"/>ISCO Companion silica chromatography, eluting with a gradient 0-100% EtOAc in cyclohexane to give the title compound.1H NMR (DMSO-d6) delta 7.18 (1 H, s), 3.85-3.77 (1 H, m), 3.69 (3H, s), 3.36-3.33 (2H, m), 3.28 (3H, s), 1.12 (3H, d), amine proton not seen.
 

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