تفاعل #586123

ord-84eda8357f904bd2a49041cb6a55a14d

معادلة التفاعل

O
water
N#Cc1ccc(-c2c[nH]nc2C(F)(F)F)cc1S
2-mercapto-4-(3-trifluoromethylpyrazolyl)benzonitrile
BrCC1CCC1
cyclobutylmethyl bromide
O=C([O-])[O-].[K+].[K+]
potassium carbonate
N#Cc1ccc(-c2c[nH]nc2C(F)(F)F)cc1SCC1CCC1
2-cyclobutylmethylthio-4-(3-trifluoromethylpyrazolyl)benzonitrile
المردود 21.6%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe resulting reaction mixture
  2. 2
    استخلاصthe organic matters were extracted with 20 ml of ethyl acetate twice
  3. 3
    غسيلwashed with 30 ml of water twice
  4. 4
    تجفيفdried over anhydrous magnesium sulfate
  5. 5
    workup.DISTILLATIONthe ethyl acetate was distilled off under reduced pressure
  6. 6
    أخرىPurification of the residue by silica gel column chromatography

الإجراء التجريبي

0.9 g (3.3 mmol) of 2-mercapto-4-(3-trifluoromethylpyrazolyl)benzonitrile, 0.5 g (3.3 mmol) of cyclobutylmethyl bromide and 0.55 g (4.0 mmol) of potassium carbonate were stirred in 5 ml of N,N-dimethylformamide at room temperature overnight. The resulting reaction mixture was poured into 50 ml of water and the organic matters were extracted with 20 ml of ethyl acetate twice. The ethyl acetate layers were combined, then washed with 30 ml of water twice and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 0.24 g of 2-cyclobutylmethylthio-4-(3-trifluoromethylpyrazolyl)benzonitrile (yield 21.2%) as a pale yellow powder (m.p. 102-103° C.).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07767626B2uspto-grants-2010_08