تفاعل #3873

ord-3d9fe4eea0d14c78998610d953418f18

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحAfter about 30 minutes the solution is filtered
  2. 2
    غسيلwashed once with water (10 ml)
  3. 3
    تجفيفdried (MgSO4)
  4. 4
    أخرىevaporated to dryness
  5. 5
    أخرىThe resulting residue is chromatographed on silica gel

الإجراء التجريبي

The N-p-methoxybenzyloxycarbonyl-D-serine benzyl ester (720 mg, 2.00 mmol) is dissolved in dry dichloromethane (20 ml) and the solution cooled to dry ice/acetone. Boron trifluoride etherate (100 μl) is added followed by the portionwise addition of diazomethane (30 mmol in 20 ml CH2Cl2). After about 30 minutes the solution is filtered and washed once with water (10 ml), then dried (MgSO4) and evaporated to dryness. The resulting residue is chromatographed on silica gel using chloroform as eluant to give the pure title compound as an oil (520 mg, 70%) which crystallises on standing to give a colourless solid of m.p. 68°-69° C.; [α]D20 -1.3° (c 4.0, CHCl3).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04722924uspto-grants-1988_02