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Water → 5-Fluoronaphthalen-1-ol

HRID 2075547
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HRID 2075547 반응식
[F:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[C:7]2[O:12]C.B(Br)(Br)Br.O>ClCCl>[F:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[C:7]2[OH:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 25134Boron tribromide2회HCID 123363901-Fluoro-5-methoxynaphthalene

생성물 1

HCID 123363915-Fluoronaphthalen-1-ol수율 83%

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

A stirred solution of 2.08 g of 5-fluoro-1-methoxynaphthalene in 42 ml of dry dichloromethane was cooled to −60 to −65° C. after which was added 13 ml of 1M BBr3 in dichloromethane. The mixture was allowed to warm to room temperature, and stirred at RT for 1 h. The reaction mixture was again cooled to −60 to −65° C. after which was added an additional 13 ml of 1M BBr3 in dichloromethane. The mixture was allowed to warm to RT and stirred at RT for 1.5 h. The mixture was poured into cold water, extracted twice with dichloromethane, dried (sodium sulphate), filtered and concentrated to a purple/white solid. The material was dissolved in a minimum volume of dichloromethane and flash chromatographed on silica gel, eluting with ethyl acetate/dichloromethane/heptane to provide 1.58 g (83%) of 5-fluoro-1-hydroxynaphthalene as a white solid.

후처리

  1. temperatureThe reaction mixture was again cooled to −60 to −65° C. after which
  2. temperatureto warm to RT
  3. stirringstirred at RT for 1.5 h
  4. extractionextracted twice with dichloromethane
  5. dry with materialdried (sodium sulphate)
  6. filtrationfiltered
  7. concentrationconcentrated to a purple/white solid
  8. dissolutionThe material was dissolved in a minimum volume of dichloromethane and flash
  9. customchromatographed on silica gel
  10. washeluting with ethyl acetate/dichloromethane/heptane

출처 및 근거

ORD 기록
ord-14f9347138da4f2eaaa35365803f9d50
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07919628B2

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