반응 #447096

ord-0da8112aec424316aed76fc8b55c3ac9

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타After evaporating volatile components off in the same manner as in Example 1
  2. 2
    workup.ADDITIONto the residue, dichloromethane (20 ml) was added
  3. 3
    workup.STIRRINGstirred at room temperature
  4. 4
    기타to obtain a homogeneous solution
  5. 5
    온도After cooling the resulting solution to 0° C.
  6. 6
    workup.STIRRINGstirred at room temperature for 15 hours
  7. 7
    workup.ADDITIONThereafter, the reaction mixture was treated in the same manner as in Example 1
  8. 8
    기타was produced in the yield of 55% which

실험 절차

To a solution of L(+)-diethyl tartarate (412 mg) in absolute dichloromethane (20 ml), tetaraisopropyl titanate (568 mg) was dropwise added and stirred at room temperature for 30 minutes. After evaporating volatile components off in the same manner as in Example 1, to the residue, dichloromethane (20 ml) was added and stirred at room temperature to obtain a homogeneous solution. After cooling the resulting solution to 0° C., hydrogen cyanide (0.4 ml) and then benzaldehyde (212 mg) were added and stirred at room temperature for 15 hours. Thereafter, the reaction mixture was treated in the same manner as in Example 1 and analyzed by HPLC to reveal that α-cyanobenzyl alcohol was produced in the yield of 55% which contained the R(+) isomer with the enantiomer excess percentage of 77%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05003083uspto-grants-1991_03