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CID 223829 → 3-Phenanthrylamine

HRID 2117975
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HRID 2117975 반응식
C1N(COCCO)[C:4]2NC(N)=[N:13][C:14](=O)[C:3]=2N=1.[CH:17]1[C:30]2C=CC3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[C:21]=2[CH:20]=[C:19](C(=NO)C)[CH:18]=1>>[CH:25]1[C:24]2[CH:23]=[CH:22][C:21]3[C:30](=[CH:17][CH:18]=[CH:19][CH:20]=3)[C:4]=2[CH:3]=[C:14]([NH2:13])[CH:26]=1
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참가 물질

3

반응물 2

HCID 223829CID 223829HCID 178508935HCID 178508935, 화합물

생성물 1

HCID 746913-Phenanthrylamine수율 92.4%

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온도
100 °C

실험 절차

To 385 g of polyphosphoric acic at 100° C. was added 32 g (0.14 mol) of 1-(3-phenanthryl)ethanone oxime from Step 1 over 30 minutes. The mixture was stirred at 100° C. for 2 hrs, cooled down to room temperature followed by the addition of water/ice. Stirred 30 minutes, filtered and washed with water. This white solid was then placed in 500 mL of methanol and 40 mL of concentrated HCl. The reaction was refluxed overnight, cooled down to room temperature and concentrated down. A mixture of ethyl acetate/water was added to the residue and the resulting solution was made basic with 10 N KOH. The aqueous layer was extracted with ethyl acetate and combined organic layers were washed with water, brine, dried over sodium sulphate and volatiles were removed under reduced pressure to afford 25 g of 3-phenanthrylamine as a beige solid.

후처리

  1. temperaturecooled down to room temperature
  2. stirringStirred 30 minutes
  3. filtrationfiltered
  4. washwashed with water
  5. temperatureThe reaction was refluxed overnight
  6. temperaturecooled down to room temperature
  7. concentrationconcentrated down
  8. additionA mixture of ethyl acetate/water
  9. additionwas added to the residue
  10. extractionThe aqueous layer was extracted with ethyl acetate
  11. washwere washed with water, brine
  12. dry with materialdried over sodium sulphate and volatiles
  13. customwere removed under reduced pressure

출처 및 근거

ORD 기록
ord-f7b5fa2c5ff34eb0b62b00f1bb48b709
출처 데이터셋
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07442716B2

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