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Dimethyl Sulfide → 4-(4-Chlorophenyl)isoxazole-3-carbaldehyde

HRID 1506652
ノート
印刷プレビュー

反応式

HRID 1506652 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9](/[CH:13]=C/C3C=CC=CC=3)=[N:10][O:11][CH:12]=2)=[CH:4][CH:3]=1.[O:21]=[O+][O-].CSC>C(Cl)Cl.CO>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:9]([CH:13]=[O:21])=[N:10][O:11][CH:12]=2)=[CH:4][CH:3]=1
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 1068Dimethyl SulfideHCID 24823OzoneHCID 90280212HCID 90280212、化合物

生成物 1

HCID 902802044-(4-Chlorophenyl)isoxazole-3-carbaldehyde

試薬・触媒・溶媒 1

HCID 21226129Dichloromethane methanol溶媒

反応条件

温度
-78 °C

実験手順

(E)-4-(4-Chlorophenyl)-3-styrylisoxazole (2 g, 7.1 mmol) was dissolved in DCM/MeOH (20 mL/2 mL) and cooled to −78° C. The reaction was placed under ozonolysis conditions (O3 bubbling) until full disappearance of starting material. DMS (8 mL) was added and the reaction was let warm to ambient temperature. After 15 h, the reaction was partitioned between EtOAc and H2O. The organics were separated, washed with saturated aqueous NaHCO3, and dried with saturated aqueous NaCl. Solvents were removed in vacuo and the residue purified by column chromatography on silica to provide the desired product: MS (m/z) 208.0 [M+H]+.

後処理

  1. temperaturethe reaction was let warm to ambient temperature
  2. customthe reaction was partitioned between EtOAc and H2O
  3. customThe organics were separated
  4. washwashed with saturated aqueous NaHCO3
  5. dry with materialdried with saturated aqueous NaCl
  6. customSolvents were removed in vacuo
  7. customthe residue purified by column chromatography on silica

出典と根拠

ORDレコード
ord-4c36f1ce27fc457e8309a2c96e55c168
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09220710B2

反応ノート

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