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Formaldehyde → 1-(4-Methoxybenzyl)-4-hydroxyethyl-3-nitro-2-pyridone

HRID 1387269
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HRID 1387269 반응식
[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-:17])=[O:16])[C:9]2=[O:18])=[CH:5][CH:4]=1.[CH2:21]=[O:22].C[O-].[Na+]>CS(C)=O.C(OCC)(=O)C>[CH3:1][O:2][C:3]1[CH:20]=[CH:19][C:6]([CH2:7][N:8]2[CH:13]=[CH:12][C:11]([CH2:14][CH2:21][OH:22])=[C:10]([N+:15]([O-:17])=[O:16])[C:9]2=[O:18])=[CH:5][CH:4]=1
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참가 물질

6

반응물 3

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

생성물 1

HCID 541704571-(4-Methoxybenzyl)-4-hydroxyethyl-3-nitro-2-pyridone수율 59.2%

시약·촉매·용매 2

HCID 679Dimethyl Sulfoxide용매
HCID 8857
Ethyl Acetate
용매

실험 절차

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%).

후처리

  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)

출처 및 근거

ORD 기록
ord-82aa670515604c0588d22b05ec52b89d
출처 데이터셋
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06268365B1

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