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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Isopropyl iodide → Benzonitrile, 3-methoxy-4-(1-methylethoxy)-

HRID 870523
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HRID 870523 반응식
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[O:10][CH3:11].C(=O)([O-])[O-].[K+].[K+].[CH:18](I)([CH3:20])[CH3:19]>CC(C)=O>[CH:18]([O:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][C:3]=1[O:10][CH3:11])([CH3:20])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6362Isopropyl iodideHCID 11430Potassium CarbonateHCID 781354-Hydroxy-3-methoxybenzonitrile

생성물 1

HCID 2125297Benzonitrile, 3-methoxy-4-(1-methylethoxy)-

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

25 g 4-Hydroxy-3-methoxy-benzonitrile, 27.8 g potassium carbonate and 33.5 mL isopropyl iodide were placed in 250 mL acetone and heated to reflux where they were maintained for 22 h. After this time the mixture was cooled to ambient temperature and concentrated under reduced pressure. The crude product was partitioned between ethyl acetate and water and the aqueous phase was separated and extracted with additional ethyl acetate. The combined organic fractions were dried, filtered and the solvent was removed from the filtrate under reduced pressure to give the title compound which was used without further purification.

후처리

  1. temperatureheated
  2. temperatureto reflux where they
  3. temperaturewere maintained for 22 h
  4. concentrationconcentrated under reduced pressure
  5. customThe crude product was partitioned between ethyl acetate and water
  6. customthe aqueous phase was separated
  7. extractionextracted with additional ethyl acetate
  8. customThe combined organic fractions were dried
  9. filtrationfiltered
  10. customthe solvent was removed from the filtrate under reduced pressure

출처 및 근거

ORD 기록
ord-e7a06437569441fda1488f5945673c62
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08969568B2

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