Trifluoroacetic anhydride → 5-(N-benzylmethylamino)-4-methyl-2-phenyloxazole

HRID 26492노트

반응식

HRID 26492 반응식
[C:1]([NH:9][CH:10]([CH3:22])[C:11]([N:13]([CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)C)=[O:12])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.F[C:24](F)(F)C(OC(=O)C(F)(F)F)=O.C(=O)([O-])[O-].[Na+].[Na+]>C(Cl)(Cl)Cl>[CH2:16]([CH2:15][NH:13][C:11]1[O:12][C:1]([C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)=[N:9][C:10]=1[CH3:22])[C:21]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:24]=1

참가 물질

5

반응물 3

HCID 9845Trifluoroacetic anhydrideHCID 10340Sodium CarbonateHCID 213236262-Benzamido-N-benzyl-N-methylpropanamide

생성물 1

HCID 213236355-(N-benzylmethylamino)-4-methyl-2-phenyloxazole수율 82.8%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

2-Benzamido-N-benzyl-N-methylpropanamide (8.0 g., 0.0269 mol.), was dissolved in dry chloroform (40 ml.) and trifluoroacetic anhydride (17.0 g., 0.0809 mol.) was added dropwise with stirring under nitrogen. The mixture was stirred for 4 hours, then sufficient anhydrous sodium carbonate was added portionwise to neutralise the acid formed. The solid was filtered off and washed with dry chloroform (2× 10 ml.). The combined filtrates were evaporated under reduced pressure to give a brown oil, which was extracted with warm pentane. The pentane solution was evaporated to give a yellow oil 6.20 g. (82.5% IR and NMR confirm the structure.

후처리

  1. stirringThe mixture was stirred for 4 hours
  2. customformed
  3. filtrationThe solid was filtered off
  4. washwashed with dry chloroform (2× 10 ml.)
  5. customThe combined filtrates were evaporated under reduced pressure
  6. customto give a brown oil, which
  7. extractionwas extracted with warm pentane
  8. customThe pentane solution was evaporated

출처 및 근거

ORD 기록
ord-2bb484fe08ba41d3b6760dcd31368688
출처 데이터셋
uspto-grants-1979_04
특허 번호
US04150143

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