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Chemical Structure| 81784-47-6 Chemical Structure| 81784-47-6

Structure of 81784-47-6

Chemical Structure| 81784-47-6

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Product Details of [ 81784-47-6 ]

CAS No. :81784-47-6
Formula : C10H11N
M.W : 145.20
SMILES Code : CC1=CC=CC2=C1C(C)=CN2
MDL No. :MFCD03095161

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Application In Synthesis of [ 81784-47-6 ]

* 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 [ 81784-47-6 ]

[ 81784-47-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4771-48-6 ]
  • [ 81784-47-6 ]
YieldReaction ConditionsOperation in experiment
43% With lithium aluminium tetrahydride; In tetrahydrofuran; for 8.5h;Reflux; A solution of <strong>[4771-48-6]4-methyl-1H-indole-3-carbaldehyde</strong> (2.200 g, 13.82 mmol) in THF (50 mL) was added to a refluxing mixture of lithium aluminum hydride (1.154 g, 30.4 mmol) in THF (50 mL) (reflux condenser fitted to a two neck flask) over 30 min. The reaction mixture was refluxed for 8 hours, cooled to room temperature and treated with diethyl ether (~50 mL). The reaction mixture was acidified to ~pH 3 with 1N HCl, while cooling in an ice bath. The reaction mixture was diluted with EtOAc (125 mL), poured into a separatory funnel and washed with water (2X 50 mL), saturated aqueous NaCl solution (50 mL), then dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated in vacuo to afford 3,4-dimethyl-1H-indole (0.870 g, 5.99 mmol, 43% yield). LC retention time 1.15 min [Method F1]. MS (E-) m/z: 146.0 (M-H).
With lithium aluminium tetrahydride; In tetrahydrofuran; for 4h;Inert atmosphere; Reflux; In a flame-dried flask under nitrogen, a solution of the Vilsmeiere-Haack product (0.39 g, 2.5 mmol) in THF (5 mL) was added dropwise to a suspension of LiAlH4 (0.19 g, 5 mmol) in THF (1.6 mL). The reaction was heated to reflux for 4 h, then cooled to room temperature and stirred overnight. The reaction was diluted with Et2O and cooled to 0 C. Water (0.19 mL) was added slowly, then 15% NaOH(aq) (0.19 mL), then water (0.6 mL) were added. The mixture was warmed to room temperature and stirred for 15 min. Some MgSO4 was added, the mixture was stirred for 15 min, filtered, and concentrated. The crude indole was carried forward without further purification.
With lithium aluminium tetrahydride; In tetrahydrofuran; at 20℃; for 8h;Cooling with ice; Green chemistry; General procedure: This method is a general method. To a dry flask, LiAlH4 (15.0 mmol) was added, and TauHF (30.0 mL) was used as a solvent. The above-mentioned crude indole-3-formaldehyde THF (30.0 mL) solution was added dropwise under ice-water bath, and the mixture was allowed to react to room temperature for about 8 hours. The reaction was completely monitored by TLC. To the flask was added 1.0 mL of ice water, and then 1.5 g of NaOH solid and 3.0 mL of water were slowly added. After the reaction was completed, the mixture was stirred at room temperature for about 15 minutes, then the solid was filtered, and the filtrate was extracted with ethyl acetate. (3X 20.0 mL). After EtOAc (EtOAc/EtOAc/EtOAc. The desired 3-methylindoles and derivatives are obtained.
 

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