Iodine → 5-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-one

HRID 601768

反応式

HRID 601768 の反応式
[Mg].Br[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[O:9][CH3:10].II.[Cl:13][C:14]1[CH:15]=[C:16]2[C:20](=[CH:21][CH:22]=1)[NH:19][C:18](=[O:23])[C:17]2=[O:24].[Cl-].[NH4+]>C(OCC)C.C1COCC1>[Cl:13][C:14]1[CH:15]=[C:16]2[C:20](=[CH:21][CH:22]=1)[NH:19][C:18](=[O:23])[C:17]2([OH:24])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[O:9][CH3:10]

参加物

8

反応物 5

HCID 807IodineHCID 113582-BromoanisoleHCID 25517Ammonium ChlorideHCID 872035-chloro-1H-indole-2,3-dioneHCID 5462224Magnesium

生成物 1

HCID 219059555-Chloro-3-hydroxy-3-(2-methoxyphenyl)indolin-2-one収率 89.2%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒2 回HCID 8028Tetrahydrofuran溶媒

反応条件

温度
21 °C

実験手順

Magnesium turnings (40 g, 1.65 mol) are introduced into diethyl ether (100 ml) and, while stirring, a solution of 2-bromoanisole (206 ml, 1.65 mol) in diethyl ether (450 ml) is added dropwise. The reaction can be initiated, if necessary, by adding iodine crystals. During the addition, the reaction mixture should boil gently. After the addition, the mixture was stirred at room temperature for 1 hour. A slurry of 5-chloroisatin (75 g, 0.41 mol) in THF (750 ml) was added to the Grignard solution while cooling slightly (temperature 18-24° C.), and the mixture was stirred at room temperature for 30 min. The reaction mixture was stirred into ammonium chloride solution and extracted several times with ethyl acetate. The combined organic phase was washed four times with water, dried over magnesium sulfate and concentrated under reduced pressure. The remaining residue was stirred with 2-propanol. The resulting precipitate was filtered off, washed with 2-propanol and diethyl ether and dried. 106 g of the desired intermediate were obtained.

後処理

  1. customThe reaction
  2. additionDuring the addition
  3. additionAfter the addition
  4. stirringthe mixture was stirred at room temperature for 1 hour
  5. stirringthe mixture was stirred at room temperature for 30 min
  6. extractionextracted several times with ethyl acetate
  7. washThe combined organic phase was washed four times with water
  8. dry with materialdried over magnesium sulfate
  9. concentrationconcentrated under reduced pressure
  10. stirringThe remaining residue was stirred with 2-propanol
  11. filtrationThe resulting precipitate was filtered off
  12. washwashed with 2-propanol and diethyl ether
  13. customdried

出典と根拠

ORDレコード
ord-d27efc37f2e44cfb8528f7a662d313bd
出典データセット
uspto-grants-2011_03
特許番号
US07902379B2

関連ノート

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