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Chemical Structure| 688798-44-9 Chemical Structure| 688798-44-9

Structure of 688798-44-9

Chemical Structure| 688798-44-9

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Product Details of [ 688798-44-9 ]

CAS No. :688798-44-9
Formula : C10H13IO
M.W : 276.11
SMILES Code : OCCCCC1=CC=C(I)C=C1
MDL No. :MFCD21243840

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Application In Synthesis of [ 688798-44-9 ]

* 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 [ 688798-44-9 ]

[ 688798-44-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 27913-58-2 ]
  • [ 688798-44-9 ]
YieldReaction ConditionsOperation in experiment
100% With borane-THF; In tetrahydrofuran; at 20℃; for 1.5h; To an ice-cooled THF (20 mL) mixture of 4- (4-iodophenyl) butanoic acid (1) (2.90 g, 10.0 mmol) was added borane-tetrahydrofuran complex (20 mL, 1.0 M, 20 mmol) dropwise over 30 min. The resulting mixture was stirred for 1.5 hr at room temperature, and then quenched with a 1: 1 HOAc/MeOH (1 mL). The solvent was stripped, and the residue was then partitioned between EtOAc and water. The organic layer was separated, washed with saturated [NAHCO3] and brine, dried over [MGS04,] and evaporated to produce a quantitative yield of the crude alcohol as an oil. To a [CH2CL2] (12 mL) mixture of the crude alcohol (1.75 g, 6.3 mmol) was added [4-METHYLMORPHOLINE] N-oxide (1.11 g, 9.5), 4 [A] powdered molecular sieves (3 g), and tetrapropylammonium [PERRUTHENATE] ("TRAP", [0.] [11 G,] 0.3 mmol). The resulting slurry was stirred for 1 hr at room temperature. The crude material was purified on silica gel (eluting with 5-50% ethyl acetate in hexane) to afford 1.11 g (64% yield) of the desired aldehyde product (2) as an oil. LCMS : m/z = 257.0 (M+H- H20).
91.6% With borane-THF; In tetrahydrofuran; at 20℃; for 3h; 2.5 g (8.6 mmol, 1 eq.) of 4-(4-Iodo-phenyl)-butyric acid was dispersed in 20 ml of THF, followed by slowly adding 15 ml of Borane-THF complex ( 1.0 M in THF, 17.2 mmol, 2 eq.) over 20 minutes, the resulting reaction solution was gradually clear and stirred at RT for 3 hours until TLC check to find no starting materials left. The reaction was quenched by MeOH and water to destroy excess BH3 and the desired product was extracted with EtOAc. After removal of solvent in vacuo, 2.2 g (7.88 mmol, 91.6% yield) of crude product 4-(4- Iodo-phenyl)-butan-l-ol was obtained as white oil, which was proved by 1H NMR and directly used for next step reaction.
With borane-THF; In methanol; at 0℃; for 2h; A solution of BORANE-TETRAHYDROFURAN (200M .) was added dropwise to a stirred solution of 4- (4-IODOPHENYL) butanoic acid (25g) at 0C under nitrogen. After 2h methanol (200MI) was added dropwise. And then the solvent was removed in vacuo. The residue was partitioned between ether and water and the organic phase was separated. The combined organic layers were dried (NA2SO4) and evaporated to give the title compound (23 g). LCMS RT = 3.34 min.
 

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