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2-Tetralone → 2-(4-Fluorophenyl)naphthalene

HRID 1284372
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HRID 1284372 반응식
[CH2:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][C:2]1=O.[F:12][C:13]1[CH:18]=[CH:17][C:16]([Mg]Br)=[CH:15][CH:14]=1>C(OCC)C>[F:12][C:13]1[CH:18]=[CH:17][C:16]([C:2]2[CH:3]=[CH:4][C:5]3[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=3)[CH:1]=2)=[CH:15][CH:14]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 682662-TetraloneHCID 178418676HCID 178418676, 화합물

생성물 1

HCID 113450772-(4-Fluorophenyl)naphthalene

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

반응 조건

온도
200 °C

실험 절차

A mixture of 14.6 g. of 2-tetralone, 20 g. of p-fluorophenyl magnesium bromide, and 200 ml. of diethyl ether is stirred for 4 hours and then refluxed for 1 hour. The mixture is acidified with the addition of 200 ml. of 1N hydrochloric acid, filtered, and extracted with diethyl ether. The extracts are combined, washed with water to neutrality, filtered, dried and evaporated. The residue, containing 2-p-fluorophenyl-3,4-dihydronaphthalene is mixed with 25 g. of 5% palladium-on-charcoal catalyst; the resulting mixture is heated to 200°C for 6 hours, cooled, diluted with 250 ml. of chloroform, filtered, and evaporated to give 2-p-fluorophenylnaphthalene.

후처리

  1. additionA mixture of 14.6 g
  2. temperaturerefluxed for 1 hour
  3. additionThe mixture is acidified with the addition of 200 ml
  4. filtrationof 1N hydrochloric acid, filtered
  5. extractionextracted with diethyl ether
  6. washwashed with water to neutrality
  7. filtrationfiltered
  8. customdried
  9. customevaporated
  10. additionThe residue, containing 2-p-fluorophenyl-3,4-dihydronaphthalene
  11. additionis mixed with 25 g
  12. temperaturecooled
  13. additiondiluted with 250 ml
  14. filtrationof chloroform, filtered
  15. customevaporated

출처 및 근거

ORD 기록
ord-d1ec7896e8f24e168b26106b83158ee5
출처 데이터셋
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03978124

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