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Chemical Structure| 166386-81-8 Chemical Structure| 166386-81-8

Structure of 166386-81-8

Chemical Structure| 166386-81-8

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Product Details of [ 166386-81-8 ]

CAS No. :166386-81-8
Formula : C7H7IO2
M.W : 250.03
SMILES Code : OC1=CC(I)=CC=C1CO

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Application In Synthesis of [ 166386-81-8 ]

* 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 [ 166386-81-8 ]

[ 166386-81-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 16870-28-3 ]
  • [ 166386-81-8 ]
YieldReaction ConditionsOperation in experiment
88% With borane; In tetrahydrofuran; water; (c) Preparation of 2-hydroxy-4-iodobenzyl alcohol: A 1M solution of borane in THF was added dropwise at 0 C. to a solution of <strong>[16870-28-3]2-hydroxy-4-iodobenzoic acid</strong> (13.2 g, 0.05 mol) in THF (100 ml). The mixture was stirred for 6 hours at room temperature and 20 ml of a solution of THF and water (1:1) were then added. After concentration on a rotary evaporator under vacuum at 40 C. The residue was extracted with ethyl acetate. The organic phase was washed with water, dried over anhydrous magnesium sulfate and concentrated on a rotary evaporator under vacuum at 40 C. The product was purified by flash chromatography on a column of silica (60% EtOAc, 40% heptane). Its properties were as follows: White solid. Mass: 11 g. Yield: 88%. 1 H NMR (CDCl3, 250 MHz): 4.50 (2H, s), 6.81 (1H, Ar, d, J=7.75 Hz), 6.99 (1H, Ar, d, J=7.75 Hz), 7.05 (1H, Ar, s), 9.06 (1H, s).
With borane-THF; In tetrahydrofuran; at 20 - 50℃; for 3h; To a solution of <strong>[16870-28-3]2-hydroxy-4-iodobenzoic acid</strong> (3.96 g) in THF (100 mL) was added IM borane-THF complex in THF (56 mL) . The mixture was stirred at room temperature for 2 hr and at 500C for 1 hr, cooled and then quenched by the addition of IN HCl. The mixture was extracted with ethyl acetate, and the extract was dried over MgSO4, passed through silica gel plough and concentrated. The residue was collected and washed with diisopropyl ether to give the title compound as colorless crystals (2.30 g) . 1H-NMR (300 MHz, CDCl3) delta: 2.19 (IH, br) , 4.84 (2H, d, J =3.0 Hz), 6.75 (IH, d, J = 7.8 Hz), 7.19 (IH, dd, J = 7.8,1.8 Hz), 7.44 (IH, d, J = 1.8 Hz).
  • 2
  • [ 166386-81-8 ]
  • [ 38170-02-4 ]
 

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