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[ CAS No. 898832-40-1 ] {[proInfo.proName]}

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Chemical Structure| 898832-40-1
Chemical Structure| 898832-40-1
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Product Details of [ 898832-40-1 ]

CAS No. :898832-40-1 MDL No. :MFCD08544330
Formula : C8H8FNO Boiling Point : No data available
Linear Structure Formula :- InChI Key :TUSAJTKBOABBTR-UHFFFAOYSA-N
M.W : 153.15 Pubchem ID :16244451
Synonyms :

Safety of [ 898832-40-1 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 898832-40-1 ]

* 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 [ 898832-40-1 ]

[ 898832-40-1 ] Synthesis Path-Upstream   1~3

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  • [ 898832-40-1 ]
YieldReaction ConditionsOperation in experiment
87% With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; Intermediate 8: 8-Fluoro-3,4-dihydro-2H-benzo[l,4]oxazineTo a stirred mixture of 8-fluoro-2H- l, 4-benzoxazin-3(4H)-one (l .Og, 0.0059mol) in THF (25mL) was added lithium aluminium hydride (7mL, 1M solution in THF) dropwise at 0°C to -5°C. The reaction mixture was stirred at room temperature for 2h and then poured onto ice and extracted with ethyl acetate. The organic phase was dried (MgS04) and the solvent removed under reduced pressure. The residue was triturated with diethyl ether to afford 8-fluoro-3,4-dihydro-2H-benzo[l,4]oxazine (0.8g, 87percent) as a dark brown solid.Mass: (ES+) 154 (M+H) + NMR: δΗ ( 6-DMSO) 3.27 (2H, m), 4.11 (2H, m), 6.05 (1H, br s), 6.34 (2H, m) and 6.58 (1H, m).
Reference: [1] Patent: WO2011/144578, 2011, A1, . Location in patent: Page/Page column 30
[2] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 16, p. 4700 - 4704
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Reference: [1] Patent: WO2011/144578, 2011, A1,
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  • [ 698984-51-9 ]
  • [ 898832-40-1 ]
Reference: [1] Patent: WO2011/144578, 2011, A1,
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