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Dimethylformamide → Methyl 5-formyl-2-methylfuran-3-carboxylate

HRID 68572
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HRID 68572 반응식
P(Cl)(Cl)(Cl)=O.[CH3:6][O:7][C:8]([C:10]1[CH:14]=[CH:13][O:12][C:11]=1[CH3:15])=[O:9].[OH-].[Na+].CN([CH:21]=[O:22])C>>[CH3:6][O:7][C:8]([C:10]1[CH:14]=[C:13]([CH:21]=[O:22])[O:12][C:11]=1[CH3:15])=[O:9]
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참가 물질

5

반응물 4

HCID 6228DimethylformamideHCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 80237Methyl 2-methylfuran-3-carboxylate

생성물 1

HCID 2779820Methyl 5-formyl-2-methylfuran-3-carboxylate

실험 절차

Phosphorus oxychloride (33 ml) is added dropwise to a solution of 2-methyl-furan-3-carboxylic acid methyl ester (25.0 g) in DMF (75 ml) under nitrogen at 0° C. After 3 h 30 at 40° C., the reaction mixture is slowly poured onto water at 0° C. and NaOH 5 N is added carefully. The mixture is extracted three times with diethyl ether. The combined organic phases are washed with a saturated aqueous solution of NaHCO3, dried over Na2SO4 and concentrated in vacuo. The crude product is purified by chromatography on silica gel eluting with a mixture of diethyl ether and ethyl acetate (3:1) to yield 5-formyl-2-methyl-furan-3-carboxylic acid methyl ester (22.36 g) as a yellow solid. MS (HPLC/MS): 169 (MH+).

후처리

  1. additionthe reaction mixture is slowly poured onto water at 0° C.
  2. extractionThe mixture is extracted three times with diethyl ether
  3. washThe combined organic phases are washed with a saturated aqueous solution of NaHCO3
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated in vacuo
  6. customThe crude product is purified by chromatography on silica gel eluting with a mixture of diethyl ether and ethyl acetate (3:1)

출처 및 근거

ORD 기록
ord-f542d4908c674ae4bded20803a914ca4
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08822466B2

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