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N-bromobutanimide → 5-Bromo-2,2-dimethyltetrahydro-4H-pyran-4-one

HRID 541472
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HRID 541472 반응식
[CH3:1][C:2]1([CH3:9])[CH2:7][C:6](=[O:8])[CH2:5][CH2:4][O:3]1.[Br:10]N1C(=O)CCC1=O.C([O-])(=O)C.[NH4+]>CCOCC.C(OCC)(=O)C>[Br:10][CH:5]1[CH2:4][O:3][C:2]([CH3:9])([CH3:1])[CH2:7][C:6]1=[O:8]
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참가 물질

6

반응물 3

HCID 67184N-bromobutanimideHCID 517165Ammonium AcetateHCID 17381592,2-Dimethyltetrahydropyran-4-one

생성물 1

HCID 682890115-Bromo-2,2-dimethyltetrahydro-4H-pyran-4-one수율 31.5%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 8857Ethyl Acetate
용매

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온도
25 °C

실험 절차

Into around-bottom flask, was placed a solution of 2,2-dimethyloxan-4-one (1.00 g, 7.80 mmol, 1.00 equiv) in ether (20 mL). N-Bromosuccinimide (1.50 g, 25.5 mmol, 3.26 equiv) was added in portions, followed by the addition of ammonium acetate (60.0 mg, 0.78 mmol, 0.10 equiv). The resulting mixture was stirred overnight at 25° C., then diluted with ethyl acetate (20 mL). The resulting mixture was washed brine (2×40 mL), dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by silica gel chromatography with ethyl acetate/petroleum ether (1:30) as the eluent to obtain the title compound as a yellow oil (508 mg, 31%).

후처리

  1. customInto around-bottom flask, was placed
  2. washThe resulting mixture was washed brine (2×40 mL)
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by silica gel chromatography with ethyl acetate/petroleum ether (1:30) as the eluent

출처 및 근거

ORD 기록
ord-f8f003754f1b4c9e8089945a3763de34
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08871790B2

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