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Phosphorus oxide (P4O10) → 2-(2-Chloro-5-nitrophenyl)oxazole

HRID 1910771
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HRID 1910771 반응식
O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.[Cl:15][C:16]1[CH:30]=[CH:29][C:28]([N+:31]([O-:33])=[O:32])=[CH:27][C:17]=1[C:18]([NH:20][CH2:21][CH:22]([O:25]C)OC)=O>CS(O)(=O)=O>[Cl:15][C:16]1[CH:30]=[CH:29][C:28]([N+:31]([O-:33])=[O:32])=[CH:27][C:17]=1[C:18]1[O:25][CH:22]=[CH:21][N:20]=1
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참가 물질

4

반응물 2

HCID 14812Phosphorus oxide (P4O10)HCID 612487142-chloro-N-(2,2-dimethoxy-ethyl)-5-nitro-benzamide

생성물 1

HCID 190776092-(2-Chloro-5-nitrophenyl)oxazole수율 94.2%

시약·촉매·용매 1

HCID 6395Methanesulfonic Acid용매

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온도
142.5 °C

실험 절차

Under nitrogen, phosphorus pentoxide (0.98 g, 6.90 mmol) was added portionwise to a slurry of 2-chloro-N-(2,2-dimethoxy-ethyl)-5-nitro-benzamide (0.5 g, 1.73 mmol) in methanesulfonic acid (5 mL) at r.t. The mixture was heated to 140-145° C. for 6 h. After cooling to r.t., the mixture was poured onto ice-water and extracted with ethyl acetate. The combined organic phases were washed with water then brine, dried over sodium sulfate, filtered and concentrated in vacuo. Further drying under high vacuum gave 2-(2-chloro-5-nitrophenyl)-oxazole (0.366 g, 94%) as a solid.

후처리

  1. temperatureAfter cooling to r.t.
  2. additionthe mixture was poured onto ice-water
  3. extractionextracted with ethyl acetate
  4. washThe combined organic phases were washed with water
  5. dry with materialbrine, dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customFurther drying under high vacuum

출처 및 근거

ORD 기록
ord-f46591ba5e434ca1b400b77a4edb6f2c
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08604029B2

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