تفاعل #792179

ord-5283e75bd5e247caa8c921cd3dadf83a

معادلة التفاعل

CC(=O)C(F)(F)F
1,1,1-Trifluoroacetone
NN=c1[nH]cccc1Cl
3-chloro-2(1H)-pyridinone hydrazone
NNc1ncccc1Cl
(3-chloro-pyridin-2-yl)-hydrazine
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
product
المردود 66.0%
CC(=NN=c1[nH]cccc1Cl)C(F)(F)F
3-chloro-2(1H)-pyridinone (2,2,2-trifluoro-1-methylethylidene)hydrazone
المردود 66.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    أخرىThe solvent was removed under reduced pressure
  3. 3
    أخرىthe mixture partitioned between ethyl acetate (100 mL) and saturated aqueous sodium carbonate solution (100 mL)
  4. 4
    أخرىThe organic layer was dried
  5. 5
    أخرىevaporated
  6. 6
    أخرىChromatography on silica gel (eluted with ethyl acetate) gave

الإجراء التجريبي

1,1,1-Trifluoroacetone (7.80 g, 69.6 mmol) was added to 3-chloro-2(1H)-pyridinone hydrazone (alternatively named (3-chloro-pyridin-2-yl)-hydrazine) (10 g, 69.7 mmol) at 20-25° C. After the addition was complete, the mixture was stirred for about 10 minutes. The solvent was removed under reduced pressure and the mixture partitioned between ethyl acetate (100 mL) and saturated aqueous sodium carbonate solution (100 mL). The organic layer was dried and evaporated. Chromatography on silica gel (eluted with ethyl acetate) gave the product as an off-white solid (11 g, 66% yield), m.p. 64-64.5° C. (after crystallization from ethyl acetate/hexanes).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09173400B2uspto-grants-2015_11