反応 #3873

ord-3d9fe4eea0d14c78998610d953418f18

反応方程式

C=[N+]=[N-]
diazomethane
CC(C)=O.O=C=O
dry ice acetone
COc1ccc(COC(=O)N[C@H](CO)C(=O)OCc2ccccc2)cc1
N-p-methoxybenzyloxycarbonyl-D-serine benzyl ester
CCOCC.FB(F)F
Boron trifluoride etherate
COC[C@@H](NC(=O)OCc1ccc(OC)cc1)C(=O)OCc1ccccc1
title compound
収率 70.0%
COC[C@@H](NC(=O)OCc1ccc(OC)cc1)C(=O)OCc1ccccc1
N-p-Methoxybenzyloxycarbonyl-O-methyl-D-serine benzyl ester
収率 70.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過After about 30 minutes the solution is filtered
  2. 2
    洗浄washed once with water (10 ml)
  3. 3
    乾燥dried (MgSO4)
  4. 4
    その他evaporated to dryness
  5. 5
    その他The resulting residue is chromatographed on silica gel

実験手順

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).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04722924uspto-grants-1988_02