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Dimethylformamide → 5-Formyl-2,4-dimethylbenzoic acid

HRID 541198
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HRID 541198 반응식
I[C:2]1[C:3]([CH3:12])=[CH:4][C:5]([CH3:11])=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8].[Li]CCCC.CN([CH:21]=[O:22])C>O1CCCC1>[CH:21]([C:2]1[C:3]([CH3:12])=[CH:4][C:5]([CH3:11])=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8])=[O:22]
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참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 230918755-Iodo-2,4-dimethylbenzoic acid2회HCID 178418339Butyllithium

생성물 1

HCID 717431195-Formyl-2,4-dimethylbenzoic acid수율 74.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-78 °C

실험 절차

To a stirred solution of 5-iodo-2,4-dimethylbenzoic acid (compound 2.1, 5 g, 18.11 mmol, 1.00 equiv) in tetrahydrofuran (150 mL) under nitrogen at −78° C. was added n-BuLi (2.5 M in THF, 18 mL, 2.50 equiv) dropwise. After stirring at −78° C. for 1 h, DMF (5 g, 68.4 mmol, 3.80 equiv) was added dropwise. The resulting mixture was stirred at −78° C. for an additional 0.5 h and then carefully quenched by slow addition of 50 mL of water. The pH was then adjusted to ˜3-4 using aqueous HCl (aq., 6 M). The mixture was extracted with 3×200 mL of ethyl acetate. The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure. The residue thus obtained was purified using silica gel column chromatography with ethyl acetate/petroleum ether (1:10-1:5) as gradient to yield 2.4 g (74%) of the title compound as a white solid.

후처리

  1. stirringThe resulting mixture was stirred at −78° C. for an additional 0.5 h
  2. customcarefully quenched by slow addition of 50 mL of water
  3. extractionThe mixture was extracted with 3×200 mL of ethyl acetate
  4. dry with materialThe combined organic layers were dried (Na2SO4)
  5. concentrationconcentrated under reduced pressure
  6. customThe residue thus obtained
  7. customwas purified

출처 및 근거

ORD 기록
ord-c5e80126c5d6463eb914dc8b8dd4b680
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08871790B2

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