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

HRID 1275663
ノート
印刷プレビュー

反応式

HRID 1275663 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 80192-Methoxyethanol溶媒

反応条件

温度
95 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-1164e58fe4b44a03800002ee524da014
出典データセット
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06162818

反応ノート

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