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Volumn , Issue 11, 2005, Pages 1801-1806

An easy access to aryl azides from aryl amines under neutral conditions

Author keywords

Amines; Anilines; Azides; Diazo compounds; Sodium azide

Indexed keywords

ELECTRONS; REACTION KINETICS; SENSITIVITY ANALYSIS; SODIUM COMPOUNDS; YIELD STRESS;

EID: 23044431612     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-869974     Document Type: Article
Times cited : (54)

References (27)
  • 7
    • 23044460109 scopus 로고
    • Klamann, D., Ed.; Thieme: Stuttgart/New York
    • (c) Hassner, A. In Houben-Weyl, Organische Stickstoffverbindungen, Vol. E16q; Klamann, D., Ed.; Thieme: Stuttgart/New York, 1990, Part I/2, 1234.
    • (1990) Houben-Weyl, Organische Stickstoffverbindungen , vol.E16Q , Issue.2 PART I , pp. 1234
    • Hassner, A.1
  • 13
    • 23044489027 scopus 로고
    • Diazotization of aryl amines in the presence of alkyl nitrite has been discussed in: Frieman, F.; Chlebowski, J. F. J. Org. Chem. 1968, 33, 1633.
    • (1968) J. Org. Chem. , vol.33 , pp. 1633
    • Frieman, F.1    Chlebowski, J.F.2
  • 14
    • 23044434685 scopus 로고    scopus 로고
    • note
    • GC analysis showed the presence of ca. 40% t-BuOH in t-BuONO. This reagent could be stored in the refrigerator (4 °C) for one week. However, t-BuONO stored more than a week was not as effective and larger excess of reagent was needed for completion of the reaction. The amount of t-BuONO was calculated on the basis of 60% purity.
  • 18
    • 23044505694 scopus 로고    scopus 로고
    • note
    • Isoamyl nitrite was purchased from Aldrich Chemical.
  • 19
    • 23044479473 scopus 로고    scopus 로고
    • note
    • 2-Aminobenzoxazole did not undergo transformation to corresponding azide under the reaction conditions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.