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Chemical Structure| 127561-11-9 Chemical Structure| 127561-11-9

Structure of 127561-11-9

Chemical Structure| 127561-11-9

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Product Details of [ 127561-11-9 ]

CAS No. :127561-11-9
Formula : C12H10FNO3
M.W : 235.21
SMILES Code : O=C(OCC)C(C1=CNC2=C1C=C(F)C=C2)=O
MDL No. :MFCD12546260

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Application In Synthesis of [ 127561-11-9 ]

* 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.

  • Downstream synthetic route of [ 127561-11-9 ]

[ 127561-11-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 127561-11-9 ]
  • [ 101349-12-6 ]
YieldReaction ConditionsOperation in experiment
100% With LiAlH4; In tetrahydrofuran; EXAMPLE 11 5-Floro-3-(2-hydroxyethyl)indole To a suspension of LiAlH4 (8.60 g, 0.23 mol) in 400 mL of dry THF was added 5-fluoro-3-indoleglyoxylic acid ethyl ester (13.50 g, 0.057 mol) portionwise at room temperature. Preparation of this ester intermediate is given hereinbelow. The mixture was heated to reflux under Ar for 1 h and was then cooled at 0 C. and quenched according to the method of Fieser (Fieser and Fieser, "Reagents for Organic Synthesis", Vol. 1, pg. 584). The resulting slurry was filtered and the filter cake was washed with THF. The filtrate was dried (Na2 SO4) and evaporated to give the product (10.00 g, 100%) as a yellow oil. It was used as such without further purification; IR (neat) 3420 cm-1
100% With LiAlH4; In tetrahydrofuran; Example 13 5-Fluoro-3-(2-hydroxyethyl)indole To a suspension of LiAlH4 (8.60 g, 0.23 mole) in 400 mL of dry THF was added 5-fluoro-3-indoleglyoxylic acid ethyl ester (13.50 g, 0.057 mole) portionwise at room temperature. Preparation of this ester intermediate is given hereinbelow. The mixture was heated to reflux under Ar for 1 h and was then cooled at 0 C. and quenched according to the method of Fieser (Fieser and Fieser, "Reagents for Organic Synthesis", Vol. 1, pg. 584). The resulting slurry was filtered and the filter cake was washed with THF. The filtrate was dried (Na2 SO4) and evaporated to give the product (10.00 g, 100%) as a yellow oil. It was used as such without further purification; IR (neat) 3420 cm-1. 1 Hnmr (80 MHz, CDCl3). delta: 7.73 (br s, 1H), 7.1-6.4 (m, 4H), 3.57 (t, J=8 Hz, 2H), 2.66 (t, J=8 Hz, 2H), 1.20 (br s, 1H).
 

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