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Chemical Structure| 3377-71-7 Chemical Structure| 3377-71-7

Structure of 3377-71-7

Chemical Structure| 3377-71-7

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Product Details of [ 3377-71-7 ]

CAS No. :3377-71-7
Formula : C15H13N
M.W : 207.27
SMILES Code : N1(CC2=CC=CC=C2)C=CC3=C1C=CC=C3
MDL No. :MFCD00015884
InChI Key :NJZQOCCEDXRQJM-UHFFFAOYSA-N
Pubchem ID :96913

Safety of [ 3377-71-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P280-P305+P351+P338-P304+P340-P405-P501

Application In Synthesis of [ 3377-71-7 ]

* 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 [ 3377-71-7 ]

[ 3377-71-7 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 27018-76-4 ]
  • [ 3377-71-7 ]
  • 2
  • [ 3377-71-7 ]
  • [ 208838-29-3 ]
  • C25H24N2O2 [ No CAS ]
  • 3
  • [ 3377-71-7 ]
  • [ 124-38-9 ]
  • [ 27018-76-4 ]
YieldReaction ConditionsOperation in experiment
98% With dimethylaluminum chloride; In hexane; toluene; at 20℃; under 22502.3 Torr; for 3h;Autoclave; General procedure: In a 50 mL autoclave equipped with a glass inner tube and a magnetic stirring bar were charged indole 1a (d 1.05; 125 mL, 1.00 mmol), Me2AlCl (1.0 M solution in hexane; 1.0 mL, 1.0 mmol), toluene (1.0 mL) under nitrogen atmosphere, and the apparatus was purged with CO2 by repeated pressurization and subsequent expansion, the final pressure being adjusted to 3.0 MPa. After the mixture was stirred at 80 C for 3 h, the reactor was allowed to cool to room temperature and depressurized. The reaction mixture was quenched with 2 M HCl and the aqueous layer was extracted with ethyl acetate. The combined organic layer was extracted with 0.5M Na2CO3 and the extract was acidified by the addition of concentrated HCl to liberate the free carboxylic acid, which was extracted with ethyl acetate. The extract was dried over MgSO4 and evaporated to leave a residue, which was purified by column chromatography with chloroform-ethyl acetate (1:1) as an eluent to give acid 2a as crystals (168 mg, 96%). The carboxylation of other indoles was conducted by a similar procedure. The crude product was routinely purified by column chromatography using chloroform-ethyl acetate (1:1) or chloroform-ethyl acetate (1:1) containing 1% (v/v) of acetic acid as an eluent. See Tables 1 and 2 for the reaction conditions and product yields.
  • 4
  • [ 3377-71-7 ]
  • [ 2150-46-1 ]
  • methyl 6-benzyl-2-hydroxy-6H-benzofuro[2,3-b]indole-1-carboxylate [ No CAS ]
 

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