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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → Ethyl (5-fluoronaphthalen-1-yl)acetate

HRID 331248
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HRID 331248 반응식
[F:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][CH:6]=[C:7]2[CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14].ClC1C(=O)C(C#N)=C(C#N)C(=O)C=1Cl>C1C=CC=CC=1.[OH-].[Na+]>[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[CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14]
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참가 물질

5

반응물 2

HCID 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 86641634Ethyl (5-fluoro-3,4-dihydronaphthalen-1-yl)acetate

생성물 1

HCID 86641635Ethyl (5-fluoronaphthalen-1-yl)acetate수율 34.8%

시약·촉매·용매 2

HCID 241Benzene용매HCID 14798Sodium Hydroxide용매

실험 절차

To a solution of ethyl (5-fluoro-3,4-dihydronaphthalen-1-yl)acetate (16.4 g) in benzene (500 mL) was DDQ (2,3-dichloro-5,6-dicyanobenzoquinone)(21.5 g), and the mixture was stirred with heating for 3 hr. After cooling, the precipitated solid was dissolved in 1N sodium hydroxide, and the mixture was extracted with toluene. The extract was washed with water and saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give ethyl (5-fluoronaphthalen-1-yl)acetate (5.66 g).

후처리

  1. temperaturewith heating for 3 hr
  2. temperatureAfter cooling
  3. extractionthe mixture was extracted with toluene
  4. washThe extract was washed with water and saturated brine
  5. dry with materialdried over magnesium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-be1c240088864f06b1c9993f86e5a1f0
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08877779B2

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