Electrochemical acetoxylation of N-acetylindolines and N-acetylindoles. A new synthesis of indigos

Sigeru Torii, Tooru Yamanaka, Hideo Tanaka

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

Electrochemical acetoxylation of N-acetylindolines 3 in AcOH-Et3N at potentials 1.1-1.7 V vs. SCE, 4 faradays/ mol of electricity, using platinum electrodes afforded the corresponding 2,3-diacetoxyindolines 5 in 70-77% yields. Likewise, N-acetylindoles 4 gave 5 in 76-82% yields. The acetate 5 could also be prepared from indoline (2) without isolating the intermediates 3 and 4. Thermal decomposition of 5 at 140-145°C gave N-acetylindoxyl acetates 7 in 81-87% yields and subsequent hydrolysis with 1 M aqueous sodium hydroxide provided indigos in 86-96% yields. Electrochemical bromination of 3a (X = H) using various alkali bromides led to the corresponding bromide 3b (X = Br) in 95-99% yields, which can be used as a precursor of bromoindigo synthesis.

Original languageEnglish
Pages (from-to)2882-2885
Number of pages4
JournalJournal of Organic Chemistry
Volume43
Issue number14
Publication statusPublished - 1978

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Bromides
Acetates
Sodium Hydroxide
Alkalies
Platinum
Hydrolysis
Pyrolysis
Electricity
Electrodes
indoline

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

Electrochemical acetoxylation of N-acetylindolines and N-acetylindoles. A new synthesis of indigos. / Torii, Sigeru; Yamanaka, Tooru; Tanaka, Hideo.

In: Journal of Organic Chemistry, Vol. 43, No. 14, 1978, p. 2882-2885.

Research output: Contribution to journalArticle

Torii, Sigeru ; Yamanaka, Tooru ; Tanaka, Hideo. / Electrochemical acetoxylation of N-acetylindolines and N-acetylindoles. A new synthesis of indigos. In: Journal of Organic Chemistry. 1978 ; Vol. 43, No. 14. pp. 2882-2885.
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