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Iodine → (3r,5r)-3-Heptyl-5-iodomethyl-dihydrofuran-2-one

HRID 1459063
ノート
印刷プレビュー

反応式

HRID 1459063 の反応式
[CH2:1]([C@H:8]([CH2:12][CH:13]=[CH2:14])[C:9]([OH:11])=[O:10])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].[I:15]I>C1COCC1.O.CCOCC>[CH2:1]([C@@H:8]1[CH2:12][C@H:13]([CH2:14][I:15])[O:10][C:9]1=[O:11])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 807IodineHCID 11041739(2R)-2-Heptyl-pent-4-enoic acid

生成物 1

HCID 10903418(3r,5r)-3-Heptyl-5-iodomethyl-dihydrofuran-2-one収率 71.1%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 21881883Oxolane--water (1/1)溶媒

実験手順

To a solution of 7.14 g (0.036 mol) of the product of Example 5 in 750 mL of THF/H2O (2:1), cooled to 0 degrees, was added 7.22 g (0.072 mol) of KHCO3 followed by 11.97 g (0.072 mol) of KI and then 18.30 g (0.072 mol) of iodine. The reaction was allowed to warm to room temperature and stirred for 18 h. The resulting mixture was diluted with ether and the organic layer was washed with aqueous sodium bisulfite solution, H2O and brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was chromatographed on silica gel eluting with ethyl acetate/hexanes (1:10) to provide 8.30 g (71%) of the title compound and 3.36 g (29%) of the corresponding iodo-trans lactone as white solids. CI Mass Spec: 325.3 (M+H).

後処理

  1. washthe organic layer was washed with aqueous sodium bisulfite solution, H2O and brine
  2. dry with materialdried over MgSO4
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customThe residue was chromatographed on silica gel eluting with ethyl acetate/hexanes (1:10)

出典と根拠

ORDレコード
ord-b4d2cb0fd3a04b658a6365e15cc4aad1
出典データセット
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05852213

反応ノート

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