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Formaldehyde → HCID 21706521、化合物

HRID 1005399
ノート
印刷プレビュー

反応式

HRID 1005399 の反応式
[CH3:1][O:2][C:3]1[CH:20]=[CH:19][C:6]([CH2:7][N:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[C:10]([N+:15]([O-])=O)[C:9]2=[O:18])=[CH:5][CH:4]=1.[CH2:21]=O.C[O-].[Na+]>CS(C)=O.C(OCC)(=O)C>[NH2:15][C:10]1[C:9](=[O:18])[N:8]([CH2:7][C:6]2[CH:19]=[CH:20][C:3]([O:2][CH3:1])=[CH:4][CH:5]=2)[CH:13]=[CH:12][C:11]=1[CH2:14][CH3:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 712FormaldehydeHCID 10942334Sodium MethoxideHCID 110111821-(4-Methoxybenzyl)-4-methyl-3-nitro-2-pyridone

生成物 1

HCID 21706521HCID 21706521、化合物収率 59.2%

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

To a stirred mixture of 1-(4-methoxybenzyl)-4-methyl-3-nitro-2-pyridone (1.38 g, 5.0 mmol) and paraformaldehyde (0.152 g) in dimethylsulfoxide (8 mL) was added sodium methoxide (0.018 g). After 2 hours, the mixture was diluted with ethyl acetate and washed with water. The aqueous phase was extracted with ethyl acetate, and the combined organic phase was dried, filtered and evaporated. The residual solid was triturated with chloroform/ethyl acetate (10 mL, 1/1) and 1-(4-methoxybenzyl)-4-hydroxyethyl-3-nitro-2-pyridone was collected by filtration (0.496 g). Fractionation of the supernatant over silica gel (chloroform/ethyl acetate to ethyl acetate/methanol 99/1) gave additional product (0.404 g) (total yield, 2.96 mmol, 59%).

後処理

  1. washwashed with water
  2. extractionThe aqueous phase was extracted with ethyl acetate
  3. customthe combined organic phase was dried
  4. filtrationfiltered
  5. customevaporated
  6. customThe residual solid was triturated with chloroform/ethyl acetate (10 mL, 1/1) and 1-(4-methoxybenzyl)-4-hydroxyethyl-3-nitro-2-pyridone
  7. filtrationwas collected by filtration (0.496 g)

出典と根拠

ORDレコード
ord-84c67cc065e543bc9de5dbeaa033aec7
出典データセット
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06054470

反応ノート

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