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Chemical Structure| 16513-67-0 Chemical Structure| 16513-67-0

Structure of 16513-67-0

Chemical Structure| 16513-67-0

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Product Details of [ 16513-67-0 ]

CAS No. :16513-67-0
Formula : C9H9NO3
M.W : 179.17
SMILES Code : OC1CC2=C(C=C([N+]([O-])=O)C=C2)C1
MDL No. :MFCD04038637

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Application In Synthesis of [ 16513-67-0 ]

* 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 [ 16513-67-0 ]

[ 16513-67-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 116530-60-0 ]
  • [ 16513-67-0 ]
YieldReaction ConditionsOperation in experiment
83% Example 1: 4-[4-(2-Hydroxy-indan-5-yl)-5-mercapto-4H-[1 ,2,4]triazol-3-yl]- 6-isopropyl-benzene-1,3-diol (Compound 4) <n="206"/>Scheme 15-nitro-indan-2-ol (b, Scheme 1)<strong>[116530-60-0]5-nitro-2-indanone</strong> (5.3g, 30mmol) was dissolved in EtOH: /-PrOH (1:1 , 15OmL). NaBH4 (1.7g, 45mmol) was added portion by portion at room temperature. The reaction mixture was stirred at r.t for additional 30 min and water was added at 0 0C (ice-water bath). The reaction mixture was extracted with EtOAc (10OmL x 3) and the combined organic layers were washed with water and brine and dried over Na2SO4. Purification of the concentrated crude product by column chromatography (EtOAc: Hexane = 4:6) afforded the title product as a pale yellow oil (4.47 g, 83%).
500 mg With methanol; sodium tetrahydroborate; at 0℃; for 1h; To a stuffed solution of <strong>[116530-60-0]5-nitroindan-2-one</strong> (500 mg, 2.824 mmol) in methanol (10 mL) was added sodium borohydride (215 mg, 5.648 mmol) at 0 C portionwise. The reaction mixture was allowed to stir at 0 C for 1 h. The reaction was monitored by TLC. After completion of reaction, the reaction mixture was concentrated under reduced pressure. The crude compound was diluted with water (200 mL) and extracted with EtOAc (2x250 mL). The combined organic layer was dried over sodium sulfate and concentrated to afford 5- nitroindan-2-ol (500 mg) which was taken to the next step without further purification.
  • 2
  • [ 16513-67-0 ]
  • [ 116530-60-0 ]
YieldReaction ConditionsOperation in experiment
62% With Dess-Martin periodane; In dichloromethane; at 0℃; for 2h; Compound 4 (1.0 g, 5.6 mmol, 1.0 eq) was added to 20 mL DCM. Dess-Martin (4.74 g, 11.2 mmol, 2.0 eq) was added at 0 C. Stir at 0 C for 2 hours. TLC showed the reaction was complete. A saturated sodium thiosulfate solution was added dropwise to the reaction solution. The organic phase was separated and the aqueous phase was extracted three times with 50 mL EA. The organic phase was washed with saturated sodium bicarbonate, water and saturated sodium chloride. The organic phase was dried over anhydrous sodium sulfate. The mixture was dried under reduced pressure, and then purified to afford compound 5 (0.62 g, yield: 62%).
 

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