تفاعل #710464

ord-8b9176addbc149a8a16572577beef07f

معادلة التفاعل

O
water
CCN(CC)CC
triethylamine
Nc1ccccn1
2-aminopyridine
O=C(O)C(F)(F)F
trifluoroacetic acid
O=C(N=c1cccc[nH]1)C(F)(F)F
2,2,2-trifluoro-N-(pyridin-2(1H)-ylidene)acetamide
المردود 71.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

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

المعالجة

  1. 1
    workup.STIRRINGthe mixture was stirred for 10 minutes
  2. 2
    أخرىThe mixture was transferred to a separatory funnel
  3. 3
    أخرىliquid separation
  4. 4
    غسيلthe organic layer was washed twice with 150 ml of water and twice with 150 ml of a 1% HCl aqueous solution
  5. 5
    تجفيفdried over anhydrous magnesium sulfate
  6. 6
    تركيزconcentrated under reduced pressure

الإجراء التجريبي

25 g (270 mmol) of 2-aminopyridine was dissolved in 200 ml of anhydrous dichloromethane, 41 ml (30 g, 300 mmol) of triethylamine was added thereto, and the mixture was cooled to 0° C. 38 ml (57 g, 270 mmol) of anhydrous trifluoroacetic acid was added dropwise thereto over 15 minutes, and the resulting mixture was stirred at room temperature for 2 hours. After the reaction was completed, the reaction solution was injected into about 100 ml of iced water, and the mixture was stirred for 10 minutes. The mixture was transferred to a separatory funnel to perform liquid separation, and the organic layer was washed twice with 150 ml of water and twice with 150 ml of a 1% HCl aqueous solution, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 36 g (yield 71%) of 2,2,2-trifluoro-N-(pyridin-2(1H)-ylidene)acetamide.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09301525B2uspto-grants-2016_04