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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Thionyl Chloride → 1-(Chlorophenylmethyl)-4-fluorobenzene

HRID 2202605
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HRID 2202605 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)O)=[CH:4][CH:3]=1.S(Cl)([Cl:18])=O>ClCCl>[Cl:18][CH:8]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:5]1[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=1
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 5707534-Fluorobenzhydrol

생성물 1

HCID 2162561-(Chlorophenylmethyl)-4-fluorobenzene수율 95.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

In dichloromethane (30 mL), (±)-(4-fluorophenyl)phenylmethanol (2.1 g, 10 mmol) synthesized in Production Example 195 was dissolved, and thionyl chloride (5.1 g, 42 mmol) was added dropwise thereto at a room temperature. After the completion of the dropping, the mixture was heated under reflux, and the completion of the reaction was confirmed by TLC. After the completion of the reaction, the reaction mixture was concentrated, diluted with ethyl acetate, and washed with water. The organic layer was dried over magnesium sulfate, and the solvent was distilled off. Thus the title compound (2.1 g, 94%) was obtained.

후처리

  1. dissolutionwas dissolved
  2. customat a room temperature
  3. temperatureAfter the completion of the dropping, the mixture was heated
  4. temperatureunder reflux
  5. customAfter the completion of the reaction
  6. concentrationthe reaction mixture was concentrated
  7. additiondiluted with ethyl acetate
  8. washwashed with water
  9. dry with materialThe organic layer was dried over magnesium sulfate
  10. distillationthe solvent was distilled off

출처 및 근거

ORD 기록
ord-5873cc4dd1494309bcc9ab90319b79c8
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09365553B2

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