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Hydrochloric Acid → ethyl (2E)-3-(3-iodophenyl)acrylate

HRID 1375650
ノート
印刷プレビュー

反応式

HRID 1375650 の反応式
[H-].[Na+].[I:3][C:4]1[CH:5]=[C:6]([CH:9]=[CH:10][CH:11]=1)[CH:7]=O.[NH4+].[Cl-].Cl.[C:15]([O:18][CH2:19][CH3:20])(=[O:17])[CH3:16]>C1COCC1.O>[I:3][C:4]1[CH:5]=[C:6](/[CH:7]=[CH:16]/[C:15]([O:18][CH2:19][CH3:20])=[O:17])[CH:9]=[CH:10][CH:11]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 313Hydrochloric AcidHCID 8857Ethyl AcetateHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 2526103-Iodobenzaldehyde

生成物 1

HCID 15508352ethyl (2E)-3-(3-iodophenyl)acrylate

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 8028Tetrahydrofuran溶媒

実験手順

To a suspension of NaH (60% dispersion in mineral oil) (120 mg, 3.0 mmol) in THF (20 mL) was added triethyl phosphonoacetate (436 μL, 2.2 mmol) dropwise. 3-iodo-benzaldehyde (465 mg, 2.0 mmol) was added after the bubbling has stopped. The reaction mixture was stirred at room temperature for 15 minutes. Solid NH4Cl was added, followed by 1N HCl to quench the reaction. The mixture was taken up in ethyl acetate and water. The organic phase was washed with aqueous NaHCO3, brine, dried (MgSO4), filtered and concentrated under reduced pressure and purified by flash chromatography on silica gel with hexane/ethyl acetate (4:1) to provide the titled compound (605 mg).

後処理

  1. customto quench
  2. customthe reaction
  3. washThe organic phase was washed with aqueous NaHCO3, brine
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. custompurified by flash chromatography on silica gel with hexane/ethyl acetate (4:1)

出典と根拠

ORDレコード
ord-7830f5fd47f14eb19757711483fc4a4c
出典データセット
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07169797B2

反応ノート

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