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Water → 4-Nitro-1,3-dihydro-2H-indol-2-one

HRID 1275663
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HRID 1275663 반응식
P(=O)(O)(O)O.Cl[C:7]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][C:14]=2[N+:16]([O-:18])=[O:17])[NH:9][CH:8]=1.[OH2:19]>COCCO>[N+:16]([C:14]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:15]=1[CH2:7][C:8](=[O:19])[NH:9]2)([O-:18])=[O:17]
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참가 물질

5

반응물 3

HCID 962WaterHCID 1004Phosphoric AcidHCID 120498633-CHLORO-4-NITRO-1H-INDOLE

생성물 1

HCID 216778744-Nitro-1,3-dihydro-2H-indol-2-one

시약·촉매·용매 1

HCID 80192-Methoxyethanol용매

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온도
95 °C

실험 절차

Phosphoric acid (35 mL of 86%) is added to a solution of 3-chloro-4-nitroindole (1.27 g, 6.46 mmol) in 2-methoxyethanol (50 mL) at 100° C. The resulting brown colored solution is stirred at 95° C. for 3.5 hours. The reaction is cooled to room temperature and then poured into 500 mL of water. The aqueous layer is extracted three times with ethyl acetate. The ethyl acetate layer is dried over magnesium sulfate, filtered and the solvents removed by rotary evaporation. The crude material is purified via silica gel column chromatography using 2% methanol/methylene chloride as the eluent. The product containing fractions are combined and the solvents removed by rotary evaporation to yield 0.90 g of slightly impure 4-nitrooxindole as an orange solid.

후처리

  1. temperatureThe reaction is cooled to room temperature
  2. extractionThe aqueous layer is extracted three times with ethyl acetate
  3. dry with materialThe ethyl acetate layer is dried over magnesium sulfate
  4. filtrationfiltered
  5. customthe solvents removed by rotary evaporation
  6. customThe crude material is purified via silica gel column chromatography
  7. additionThe product containing fractions
  8. customthe solvents removed by rotary evaporation

출처 및 근거

ORD 기록
ord-1164e58fe4b44a03800002ee524da014
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06162818

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