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Isopropanol → 1-(2-Chloro-1-cyclopentenyl)ethanol

HRID 2111010
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HRID 2111010 반응식
[Cl:1][C:2]1[CH2:6][CH2:5][CH2:4][C:3]=1[CH:7]=[O:8].[CH3:9][Mg]Br.C(O)(C)C>O1CCCC1>[Cl:1][C:2]1[CH2:6][CH2:5][CH2:4][C:3]=1[CH:7]([OH:8])[CH3:9]
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참가 물질

5

반응물 3

HCID 3776IsopropanolHCID 123899702-Chlorocyclopent-1-ene-1-carbaldehydeHCID 178418573HCID 178418573, 화합물

생성물 1

HCID 141843891-(2-Chloro-1-cyclopentenyl)ethanol수율 41.6%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Under an argon atmosphere, 2-chloro-1-cyclopentenecarbaldehyde (630 mg, 4.82 mmol) was dissolved in anhydrous tetrahydrofuran (19 ml), methylmagnesium bromide (1.4M toluene solution, 4.1 ml) was added dropwise at 0° C., and the mixture was stirred at room temperature for 30 minutes. Isopropanol (2 ml) was added at 0° C., and the solvent was evaporated under reduced pressure. 1N Hydrochloric acid was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (hexane:ethyl acetate=10:1-6:1) to give the title compound (294 mg, 2.01 mmol, 41.6%).

후처리

  1. customthe solvent was evaporated under reduced pressure
  2. addition1N Hydrochloric acid was added
  3. extractionthe mixture was extracted with ethyl acetate
  4. washThe organic layer was washed with saturated aqueous sodium chloride solution
  5. dry with materialdried over anhydrous sodium sulfate
  6. customThe solvent was evaporated under reduced pressure
  7. customthe residue was purified by silica gel chromatography (hexane:ethyl acetate=10:1-6:1)

출처 및 근거

ORD 기록
ord-6b7a704ec95a4182aae2e8c3e4be803a
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07517996B2

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