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Iodine → Ethyl 2-(4-hydroxyoxan-4-yl)acetate

HRID 735748
ノート
印刷プレビュー

反応式

HRID 735748 の反応式
[O:1]1[CH2:6][CH2:5][C:4](=[O:7])[CH2:3][CH2:2]1.II.Br[CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13].S(=O)(=O)(O)O>O1CCCC1.[Zn]>[OH:7][C:4]1([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH2:5][CH2:6][O:1][CH2:2][CH2:3]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 807IodineHCID 1118Sulfuric AcidHCID 7748Ethyl bromoacetateHCID 121599Tetrahydro-4H-pyran-4-one

生成物 1

HCID 21936035Ethyl 2-(4-hydroxyoxan-4-yl)acetate収率 69.3%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒
このページの内容参加物実験手順後処理出典と根拠反応ノート
HCID 8028
Tetrahydrofuran
溶媒

実験手順

To a solution of tetrahydro-4H-pyran-4-one (5.5 g, 51.6 mmol), a zinc powder (4.05 g, 61.9 mmol) and a small amount of iodine in tetrahydrofuran (60 ml) was added dropwise ethyl bromoacetate (6.28 ml, 56.7 mmol) under a nitrogen atmosphere. After heating under reflux for 6 hrs., 10% sulfuric acid (50 ml) was carefully added under ice-cooling and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate solution, dried over anhydrous MgSO4 and concentrated under reduced pressure to give the title compound (6.73 g, 69%) as a colorless oil.

後処理

  1. temperatureAfter heating
  2. temperatureunder reflux for 6 hrs
  3. temperaturecooling
  4. extractionthe mixture was extracted with ethyl acetate
  5. washThe extract was washed with saturated aqueous sodium hydrogen carbonate solution
  6. dry with materialdried over anhydrous MgSO4
  7. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-ccb328de8a8c4417bd2588f7bb8262d5
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07592453B2

反応ノート

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