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Acetate → HCID 13123247、化合物

HRID 2399696
ノート
印刷プレビュー

反応式

HRID 2399696 の反応式
C([S:8][C:9]1[C:16]([O:17][CH3:18])=[CH:15][CH:14]=[CH:13][C:10]=1[CH:11]=O)C1C=CC=CC=1.Cl.[NH2:20]O.C([O-])(=O)C.O>C(O)C>[CH3:18][O:17][C:16]1[C:9]2[S:8][N:20]=[CH:11][C:10]=2[CH:13]=[CH:14][CH:15]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 175AcetateHCID 962WaterHCID 443297Hydroxyamine hydrochlorideHCID 19384357HCID 19384357、化合物

生成物 1

HCID 13123247HCID 13123247、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

5 g of 2-benzylthio-3-methoxybenzaldehyde are dissolved in 40 ml of ethanol, and 3.9 g of hydroxylamine hydrochloride are added. 40 ml of acetate buffer (pH=5) are added to this solution, and the mixture is stirred for 30 minutes at room temperature. The mixture is poured into water and extracted using ethyl acetate. The organic phase is washed using saline, dried over sodium sulfate, filtered and concentrated. The resulting oil is added to a suspension of 1.6 g of phosphorus pentoxide in20 ml of methanesulfonic acid, and the mixture is stirred overnight at room temperature. The reaction mixture is poured onto ice and extracted using ethyl acetate. The organic phase is washed with saturated sodium hydrogen carbonate solution and with saline and dried over sodium sulfate, filtered and concentrated. After purification by chromatography, 7-methoxybenzisothiazole is obtained in the form of an oil.

後処理

  1. extractionextracted
  2. washThe organic phase is washed
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. additionThe resulting oil is added to a suspension of 1.6 g of phosphorus pentoxide in20 ml of methanesulfonic acid
  7. stirringthe mixture is stirred overnight at room temperature
  8. additionThe reaction mixture is poured onto ice
  9. extractionextracted
  10. washThe organic phase is washed with saturated sodium hydrogen carbonate solution and with saline
  11. dry with materialdried over sodium sulfate
  12. filtrationfiltered
  13. concentrationconcentrated
  14. customAfter purification by chromatography

出典と根拠

ORDレコード
ord-8f3d905014ee441f924c1fd60661ec0e
出典データセット
uspto-grants-1995_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05451595

反応ノート

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