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  • Potassium iodide catalyzed simultaneous C3-formylation and N-aminomethylation of indoles with 4-substituted-N,N-dimethylanilines.

Potassium iodide catalyzed simultaneous C3-formylation and N-aminomethylation of indoles with 4-substituted-N,N-dimethylanilines.

Organic & biomolecular chemistry (2012-11-13)
Lan-Tao Li, Hong-Ying Li, Li-Juan Xing, Li-Juan Wen, Peng Wang, Bin Wang
ABSTRACT

A one-pot dual functionalization of indoles has been developed. The simultaneous C3-formylation and N-aminomethylation of indoles can be achieved using readily available potassium iodide as a catalyst and tert-butyl peroxybenzoate as a co-oxidant.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Potassium iodide, ≥99.99% trace metals basis
Sigma-Aldrich
4-tert-Butyl-N,N-dimethylaniline, 98%
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Potassium iodide, BioUltra, ≥99.5% (AT)
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N-Methylaniline, purum, ≥98.0% (GC)
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N-Methylaniline, 98%
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N-Methylaniline, ≥99%
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Potassium iodide, suitable for plant cell culture
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Potassium iodide, BioXtra, ≥99.0%
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Potassium iodide, tested according to Ph. Eur.
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Potassium iodide, JIS special grade, ≥99.5%
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Potassium iodide, SAJ first grade, ≥99.5%
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Potassium iodide, AnhydroBeads, −10 mesh, 99.998% trace metals basis
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Potassium iodide, puriss. p.a., reag. ISO, reag. Ph. Eur., ≥99.0%
Supelco
N-Methylaniline, analytical standard
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Potassium iodide, ReagentPlus®, 99%
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Potassium iodide, ACS reagent, ≥99.0%
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Potassium iodide, puriss., meets analytical specification of Ph. Eur. BP, USP, 99.0-100.5% (calc. to the dried substance)
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Gold etchant, standard