A novel one-pot conversion of allyl alcohols into primary allyl halides mediated by acetyl halide

KİSHALI N., POLAT M., Altundas R., KARA Y.

HELVETICA CHIMICA ACTA, cilt.91, sa.1, ss.67-72, 2008 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 91 Sayı: 1
  • Basım Tarihi: 2008
  • Doi Numarası: 10.1002/hlca.200890014
  • Dergi Adı: HELVETICA CHIMICA ACTA
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.67-72
  • Atatürk Üniversitesi Adresli: Evet

Özet

A new and simple method for the synthesis of the primary allyl chlorides and bromides 9-16 from the secondary or tertiary allyl alcohols 3-8 and acyl halide was developed (Scheme 2, Table 1). Non-commercially available secondary and tertiary allyl alcohols were synthesized from the related ketones and aldehydes via the addition of vinylmagnesium chloride. Mechanistic studies indicate that the alcohols were first acetylated by the acetyl halide and then protonated prior to substitution by the halide, Cl- or Br-, via an S(N)2' reaction, to yield the primary halides (Scheme 5).