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Hydrochloric Acid → 4,5-Dichloro-2-fluorobenzaldehyde

HRID 515086
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HRID 515086 반응식
[Cl:1][C:2]1[C:13]([Cl:14])=[CH:12][C:5]([C:6](N(OC)C)=[O:7])=[C:4]([F:15])[CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].Cl>C1COCC1.O>[Cl:1][C:2]1[C:13]([Cl:14])=[CH:12][C:5]([CH:6]=[O:7])=[C:4]([F:15])[CH:3]=1
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 21226445Aluminium lithium hydrideHCID 903153424,5-dichloro-2-fluoro-N-methoxy-N-methyl-benzamide

생성물 1

HCID 873173724,5-Dichloro-2-fluorobenzaldehyde

시약·촉매·용매 2

HCID 962Water용매2회HCID 8028Tetrahydrofuran용매2회
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온도
25 °C

실험 절차

To a stirring solution of 4,5-dichloro-2-fluoro-N-methoxy-N-methyl-benzamide (5.1 g, 20.23 mmol) in THF (100 mL) at −78° was added a solution of lithium aluminum hydride in THF (12.14 mL of 2 M, 24.28 mmol). After 3 h at −78° C., 50 mL water was added followed by 50 mL of 1N HCl. The reaction was allowed to warm to 25° C. and stirred for 1 h. The reaction was diluted with water and extracted with diethyl ether. The ether was dried over Na2SO4, filtered, and concentrated to provide crude 4,5-dichloro-2-fluoro-benzaldehyde that was taken directly into the next step without further purification.

후처리

  1. extractionextracted with diethyl ether
  2. dry with materialThe ether was dried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-14102fcf9ac840ddaf6057f3fd58ecfc
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09108903B2

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