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

HRID 550283
ノート
印刷プレビュー

反応式

HRID 550283 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-4cb1496c2e9c4a728e8e5e5e96511a7c
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07943770B2

反応ノート

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