Sodium Thiosulfate → 4,4,4-Trifluoro-2-methylbutanal

HRID 2266867노트

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HRID 2266867 반응식
[CH3:1][CH:2]([CH2:5][C:6]([F:9])([F:8])[F:7])[CH2:3][OH:4].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.[O-]S([O-])(=S)=O.[Na+].[Na+].C(=O)(O)[O-].[Na+]>C(Cl)Cl.O.C(OCC)C>[CH3:1][CH:2]([CH2:5][C:6]([F:9])([F:8])[F:7])[CH:3]=[O:4]

참가 물질

8

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온도
25 °C

실험 절차

To 2-methyl-4,4,4-trifluoro-1-butanol (7.5 g, 53 mmol) in methylene chloride (CH2Cl2) (125 mL) at 0° C. was added Dess-Martin periodinane (26.5 g, 63.3 mmol). The reaction mixture was warmed to 25° C. and stirred for 20 min. To this mixture was added diethyl ether (Et2O—200 mL) followed by a solution of Na2S2O3 (29.0 g, 185 mmol) in a saturated aqueous solution of sodium bicarbonate (NaHCO3) (200 mL) and 100 mL of water. The milky white mixture was stirred until both phases were homogeneous. The phases were separated and the organic extract was washed with saturated aqueous NaHCO3 (25 mL) and aqueous 1 N Na2S2O3 (25 mL) and dried using magnesium sulfate (MgSO4). Solvents were removed by distillation at atmospheric pressure to give 2-methyl-4,4,4-trifluorobutanal (6.5 g, 88%). 1H nuclear magnetic resonance (NMR) spectrum matched that which was reported in the literature (J. Fluorine Chem. 36: 163-170 (1987).

후처리

  1. stirringThe milky white mixture was stirred until both phases
  2. customThe phases were separated
  3. extractionthe organic extract
  4. washwas washed with saturated aqueous NaHCO3 (25 mL) and aqueous 1 N Na2S2O3 (25 mL)
  5. customdried
  6. customSolvents were removed by distillation at atmospheric pressure

출처 및 근거

ORD 기록
ord-bc19b7b8c9654000aa3d711aca09e981
출처 데이터셋
uspto-grants-2010_12
특허 번호
US07858658B2

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