تفاعل #215384

ord-07c5a7bbf3e042ecad9e6da09d899969

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىto give a syrup which
  2. 2
    غسيلeluted with 2-5% ethyl acetate in chloroform
  3. 3
    تركيزconcentrated to dryness
  4. 4
    أخرىCrystallization from aqueous ethanol

الإجراء التجريبي

A solution of 2,3,4-tri-O-acetyl-1-thio-β-L-fucopyranose (2.0 g, 6.5 mmol) and 1-bromohexadecane (2.0 g, 6.5 mmol) in dichloromethane (40 ml) containing triethylamine (1 ml) is kept under nitrogen for 2 days at room temperature. The reaction is worked up in the usual manner to give a syrup which is put on a silica gel column and eluted with 2-5% ethyl acetate in chloroform. The desired fractions are pooled and concentrated to dryness. Crystallization from aqueous ethanol gives hexadecyl 2,3,4-tri-O-acetyl-1-thio-β-L-fucopyranoside (1.9 g, 55%), m.p. 49°-50°, [α]D +9° (c, 1.5, chloroform).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04259324uspto-grants-1981_03