Ammonium Chloride → 4-Methoxy-3-(3,3,3-trifluoropropyl)benzaldehyde dimethyl acetal

HRID 2308426

반응식

HRID 2308426 반응식
[Mg].I[CH2:3][CH2:4][C:5]([F:8])([F:7])[F:6].[Cl-].[NH4+].[CH3:11][O:12][CH:13]([O:22][CH3:23])[C:14]1[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[CH:16][CH:15]=1>C1COCC1.[Cu]I.C(OCC)(=O)C>[CH3:11][O:12][CH:13]([O:22][CH3:23])[C:14]1[CH:19]=[CH:18][C:17]([O:20][CH3:21])=[C:16]([CH2:3][CH2:4][C:5]([F:8])([F:7])[F:6])[CH:15]=1

참가 물질

8

반응물 4

HCID 25517Ammonium ChlorideHCID 75140p-(Dimethoxymethyl)anisoleHCID 1561651,1,1-Trifluoro-3-iodopropaneHCID 5462224Magnesium2회

생성물 1

HCID 225748774-Methoxy-3-(3,3,3-trifluoropropyl)benzaldehyde dimethyl acetal

시약·촉매·용매 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 8028Tetrahydrofuran용매HCID 8857Ethyl Acetate용매

반응 조건

온도
60 °C

실험 절차

A solution of 229A (15.8 g, 60 mmol) in dry THF (120 ml) was added to magnesium turnings (4.1 g, 170 mmol) at RT. The mixture was heated to 60° C. for 5 min, which initiated an exothermic reaction. The heating bath was removed and the mixture was allowed to reflux gently. Upon subsidence of the reaction (approximately 5 min), the mixture was heated to reflux for an additional 20 min and then was allowed to cool to RT. The clear green supernatant was transferred via canula away from excess magnesium and into a separate flask containing copper (I) iodide (575 mg, 3.0 mmol) under a nitrogen atmosphere. To this mixture was added 1-iodo-3,3,3-trifluoropropane (15 g, 67 mmol) and the resulting mixture was allowed to stir for 16 h, during which time a thick white precipitate developed. Aqueous ammonium chloride solution, ethyl acetate, and hexanes were added, and the organic layer was dried over sodium sulfate. Evaporation followed by silica gel chromatography of the residue using 3:1 hexanes/ethyl acetate as eluant provided 7.7 g of a mobile, slightly yellow oil, which was a 6:1 (mol ratio) mixture of 229B and 4-methoxybenzaldehyde dimethyl acetal, as determined by proton NMR. This mixture was used without further purification.

후처리

  1. customan exothermic reaction
  2. customThe heating bath was removed
  3. temperatureto reflux gently
  4. customUpon subsidence of the reaction (approximately 5 min)
  5. temperaturethe mixture was heated
  6. temperatureto reflux for an additional 20 min
  7. temperatureto cool to RT
  8. dry with materialthe organic layer was dried over sodium sulfate
  9. customEvaporation
  10. customprovided 7.7 g of a mobile, slightly yellow oil, which
  11. customThis mixture was used without further purification

출처 및 근거

ORD 기록
ord-25b08963229441618a79e2b5a4cf05aa
출처 데이터셋
uspto-grants-2004_12
특허 번호
US06835741B2

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