تفاعل #2389093

ord-b8f7cdcbc29a41659fd19fb538efcc7a

معادلة التفاعل

O=C1OC(=O)c2c(F)c(F)c(F)c(F)c21
tetrafluorophthalic anhydride
C[C@H](N)c1ccccc1
(S)-α-methylbenzylamine
C[C@@H](C1CCCCC1)N1C(=O)c2c(F)c(F)c(F)c(F)c2C1=O
desired product
المردود 65.3%
C[C@@H](C1CCCCC1)N1C(=O)c2c(F)c(F)c(F)c(F)c2C1=O
(S)-2-(1-cyclohexylethyl)-4,5,6,7-tetrafluoro-1H-isoindole-1,3-dione
المردود 65.3%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
180°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةAfter cooled
  2. 2
    أخرىpurified by silica gel column chromatography (eluent; methylene chloride:methanol=30:1 v/v)
  3. 3
    أخرىrecrystallized from a mixed solvent of n-hexane-ethyl acetate

الإجراء التجريبي

220 mg of tetrafluorophthalic anhydride and 127 mg of (S)-α-methylbenzylamine were charged in an egg-plant type flask of 50 ml, followed by stirring under heating at a temperature of 180° C. for 1.5 hours. After cooled, the reaction product was dissolved in chloroform, purified by silica gel column chromatography (eluent; methylene chloride:methanol=30:1 v/v), recrystallized from a mixed solvent of n-hexane-ethyl acetate, to obtain 215 mg of the desired product as a colorless powder. Yield: 65%. m.p. 147-148° C.; [α]20D=5.26° (C=0.618 AcOEt); MS(EI+) 329(M)+

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06429212B1uspto-grants-2002_08