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

HRID 541472
ノート
印刷プレビュー

反応式

HRID 541472 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 8857Ethyl Acetate
溶媒

反応条件

温度
25 °C

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-f8f003754f1b4c9e8089945a3763de34
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08871790B2

反応ノート

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