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

HRID 1506652
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HRID 1506652 반응식
[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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1068Dimethyl SulfideHCID 24823OzoneHCID 90280212HCID 90280212, 화합물

생성물 1

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

시약·촉매·용매 1

HCID 21226129Dichloromethane methanol용매

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온도
-78 °C

실험 절차

(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]+.

후처리

  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

출처 및 근거

ORD 기록
ord-4c36f1ce27fc457e8309a2c96e55c168
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09220710B2

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