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Benzaldehyde → HCID 10086774、化合物

HRID 1900220
ノート
印刷プレビュー

反応式

HRID 1900220 の反応式
[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:9][O:10][C:11]1[CH:17]=[CH:16][C:14]([NH2:15])=[CH:13][CH:12]=1.C(N(CC)CC)C.[C:25]([O:28][CH2:29][C:30](Cl)=[O:31])(=[O:27])[CH3:26]>C(Cl)Cl.CCCCCC>[CH3:9][O:10][C:11]1[CH:17]=[CH:16][C:14]([N:15]2[C@H:1]([C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[C@H:29]([O:28][C:25](=[O:27])[CH3:26])[C:30]2=[O:31])=[CH:13][CH:12]=1
参加物反応条件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 240BenzaldehydeHCID 7732P-AnisidineHCID 8471TriethylamineHCID 26297Acetoxyacetyl chloride

生成物 1

HCID 10086774HCID 10086774、化合物収率 68%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒3 回
HCID 8058
Hexane
溶媒

反応条件

温度
25 °C

実験手順

To a solution of 962 mg (4.56 mmol) of the imine derived from benzaldehyde and p-methoxy aniline, and 0.85 mL (6.07 mmol) of triethylamine in 15 mL of CH2Cl2 at -20° C. was added dropwise a solution of 413 mg (3.04 mmol) of α-acetoxy acetyl chloride in 15 mL of CH2Cl2. The reaction mixture was allowed to warm to 25° C. over an 18 h period. The reaction mixture was then diluted with 100 mL of CH2Cl2 and the solution was extracted with 30 mL of 10% aqueous HC1. The organic layer was washed with 30 mL of water and 30 mL of saturated aqueous sodium bicarbonate, dried over sodium sulfate, and concentrated to provide a solid mass. The solid was titurated with 50 mL of hexane and the mixture was filtered. The remaining solid was recrystallized from ethyl acetate/hexane to give 645 mg (68%) of cis-1-p-methoxyphenyl-3-acetoxy-4-phenylazetidin-2-one as white crystals, m.p. 163° C.

後処理

  1. extractionthe solution was extracted with 30 mL of 10% aqueous HC1
  2. washThe organic layer was washed with 30 mL of water and 30 mL of saturated aqueous sodium bicarbonate
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated
  5. customto provide a solid mass
  6. filtrationthe mixture was filtered
  7. customThe remaining solid was recrystallized from ethyl acetate/hexane

出典と根拠

ORDレコード
ord-cb889c05fce445b3b68d11a0328fc165
出典データセット
uspto-grants-1996_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05574156

反応ノート

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