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Acetic Acid → HCID 9859076、化合物

HRID 1045652
ノート
印刷プレビュー

反応式

HRID 1045652 の反応式
[C:1]1(=[O:13])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][C:2]1=[N:11]O.[C:14](O)(=[O:16])[CH3:15]>C(OC(=O)C)(=O)C.[Zn]>[O:13]=[C:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][CH:2]1[NH:11][C:14](=[O:16])[CH3:15]
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 176Acetic AcidHCID 6813148HCID 6813148、化合物

生成物 1

HCID 9859076HCID 9859076、化合物収率 66%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 7918Acetic Anhydride溶媒

実験手順

Zinc powder (24 g, 367 mmol) was added to a solution of 3,4-dihydro-[1,2]naphthoquinone 2-oxime (21.5 g, 123 mmol) in acetic acid (200 mw) and acetic anhydride (150 ml), and the solution was stirred at room temperature for 12 hours. After filtration and removal of the solvents under reduced pressure, the residue was partitioned between water and chloroform. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. After removal of the solvent, the residue was washed with ethyl acetate and dried to afford N-(1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)-acetamide (16.5 g, 81 mmol, 66%) as brown crystals.

後処理

  1. filtrationAfter filtration and removal of the solvents under reduced pressure
  2. customthe residue was partitioned between water and chloroform
  3. washThe organic layer was washed with brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customAfter removal of the solvent
  6. washthe residue was washed with ethyl acetate
  7. customdried

出典と根拠

ORDレコード
ord-14810c1b78c149e2ad3146ee4c605435
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08569294B2

反応ノート

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