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Formaldehyde → HCID 69152202、化合物

HRID 2375351
ノート
印刷プレビュー

反応式

HRID 2375351 の反応式
[C:1]([C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][NH:17][C:18](=[O:20])[CH3:19])=[CH:11][CH:10]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(=O)(=O)(O)O.[CH2:26]=O>C(O)(=O)C>[C:18]([N:17]1[CH2:16][CH2:15][C:12]2[C:11](=[CH:10][C:9]([C:1]([C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)=[O:8])=[CH:14][CH:13]=2)[CH2:26]1)(=[O:20])[CH3:19]
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 3

HCID 712FormaldehydeHCID 1118Sulfuric AcidHCID 22445845HCID 22445845、化合物

生成物 1

HCID 69152202HCID 69152202、化合物収率 34.8%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

N-[2-(4-Benzoylphenyl)ethyl]acetamide (16.46 mmol, 4.40 g) was introduced into glacial acetic acid (20 ml). Concentrated sulfuric acid (25 ml) and then formalin (49.29 mmol, 4.00 g) were slowly added thereto at 30° C. The mixture was stirred for 2 days and poured into ice-water, and the aqueous phase was extracted with ethyl acetate. The organic phase was washed with aqueous sodium carbonate solution, dried and concentrated. The residue was stirred with diethyl ether and the solid resulting therefrom was filtered off with suction. 1.6 g of the title compound were obtained as a beige-colored solid with a melting point of 110-113° C.

後処理

  1. customat 30° C
  2. extractionthe aqueous phase was extracted with ethyl acetate
  3. washThe organic phase was washed with aqueous sodium carbonate solution
  4. customdried
  5. concentrationconcentrated
  6. stirringThe residue was stirred with diethyl ether
  7. customthe solid resulting
  8. filtrationtherefrom was filtered off with suction

出典と根拠

ORDレコード
ord-77f4301a5a4a4350bd680a09f31053cb
出典データセット
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07465744B2

反応ノート

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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