تفاعل #2028950

ord-61b9eae2e216421a8218e6a57e054dd4

معادلة التفاعل

CC1(C)COc2c(F)c(F)cc3c(=O)c(C(=O)O)cn1c23
8
CC1(C)COc2c(F)c(F)cc3c(=O)c(C(=O)O)cn1c23
9,10-Difluoro-3,3-dimethyl-7-oxo-3,7-dihydro-2H-(1,4)oxazino(2,3,4-ij)quinoline-6-carboxylic acid
O=[N+]([O-])[O-].[K+]
KNO3
CC1(C)COc2c(F)c(F)c([N+](=O)[O-])c3c(=O)c(C(=O)O)cn1c23
9
المردود 87.9%
CC1(C)COc2c(F)c(F)c([N+](=O)[O-])c3c(=O)c(C(=O)O)cn1c23
9,10-difluoro-3,3-dimethyl-8-nitro-7-oxo-3,7-dihydro-2H-(1,4)oxazino(2,3,4-ij)quinoline-6-carboxylic acid
المردود 87.9%

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe resulting precipitate was removed by filtration
  2. 2
    غسيلwashed with ice-cold water
  3. 3
    أخرىThe resulting solid was dried

الإجراء التجريبي

A solution of 8 (7.5 g, 25.4 mmol) in concentrated H2SO4 (30 mL) was treated portionwise at 0° C. with solid KNO3 (3.9 g, 38.6 mmol). After stirring at 0° C. for 2 h, the reaction mixture was poured into 500 mL of ice-water and the resulting precipitate was removed by filtration and washed with ice-cold water. The resulting solid was dried to yield 9 as a yellow solid (7.6 g, 87% yield).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08389514B2uspto-grants-2013_03