تفاعل #460538

ord-59bbdc689ce24ee88b2bfe0a985a3868

معادلة التفاعل

C=C[C@H]1CN2CC[C@H]1C[C@H]2[C@H](O)c1ccnc2ccccc12
Cinchonidine
CC(C(=O)O)c1cccc(C(=O)c2ccccc2)c1
racemic ketoprofen
CCOC(C)=O
ethyl acetate
C=C[C@H]1CN2CC[C@H]1C[C@H]2[C@H](O)c1ccnc2ccccc12.C[C@H](C(=O)O)c1cccc(C(=O)c2ccccc2)c1
salt
المردود 31.0%
C=C[C@H]1CN2CC[C@H]1C[C@H]2[C@H](O)c1ccnc2ccccc12.C[C@H](C(=O)O)c1cccc(C(=O)c2ccccc2)c1
(S)-(-)-Ketoprofen cinchonidine
المردود 31.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
35°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىcrystallization
  2. 2
    workup.STIRRINGAfter stirring at room temperature for 16 h and 0° C. for 5-6 h
  3. 3
    ترشيحthe precipitated diastereomeric salt was filtered under vacuum
  4. 4
    غسيلwashed three times with ethyl acetate and three times with ether
  5. 5
    أخرىdried under vacuum for 16 h [Yield: 127 g (or 44%); enantiomeric purity: 86% S]
  6. 6
    أخرىOne recrystallization from 1.7 L of ethyl acetate/methanol (10:1)

الإجراء التجريبي

Cinchonidine (155 g; 0.53 mol) was added to a solution of 115g (0.59 mol) of racemic ketoprofen and 2.8 L of ethyl acetate under vigorous stirring at 50°-60° C. The mixture was diluted with 280 mL of methanol, cooled to 35° C., then seeded with 98% enantiomerically pure S-salt to induce crystallization. After stirring at room temperature for 16 h and 0° C. for 5-6 h, the precipitated diastereomeric salt was filtered under vacuum, washed three times with ethyl acetate and three times with ether, and then dried under vacuum for 16 h [Yield: 127 g (or 44%); enantiomeric purity: 86% S]. One recrystallization from 1.7 L of ethyl acetate/methanol (10:1) afforded 88 g (31% yield) salt of 97% enantiomerically pure S-ketoprofen.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05162576uspto-grants-1992_11