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Sodium Hydroxide → (NE)-N-(1,1,1-trifluorobutan-2-ylidene)hydroxylamine

HRID 906204
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HRID 906204 반응식
[F:1][C:2]([F:8])([F:7])[C:3](=O)[CH2:4][CH3:5].Cl.[NH2:10][OH:11].[OH-].[Na+]>O>[F:1][C:2]([F:8])([F:7])/[C:3](=[N:10]/[OH:11])/[CH2:4][CH3:5]
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참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 2382881,1,1-Trifluorobutan-2-oneHCID 443297Hydroxyamine hydrochloride

생성물 1

HCID 13620728(NE)-N-(1,1,1-trifluorobutan-2-ylidene)hydroxylamine수율 44.5%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

To a solution of 1,1,1-trifluorobutan-2-one (5.0 g, 39.9 mmol) and hydroxylamine hydrochloride (3.22 g, 46.3 mmol) in water (28 mL) was added a solution of sodium hydroxide (1.84 g, 46.0 mmol) in water (14 mL), then the mixture was brought to reflux for 4 hr. After cooling to room temperature, the mixture was extracted with dichloromethane (3×50 mL) and the combined organic layers were washed with water, brine, then dried over anhydrous sodium sulfate. Filtration and concentration then distillation using a 10 cm Vigreux column (b.p. 123-124° C.) afforded (E)-1,1,1-trifluorobutan-2-one oxime (2.50 g, 44.5% yield) as a clear liquid. 1H NMR (400 MHz, CDCl3): 9.18 (br s, 1H), 2.52 (q, 2H), 1.21 (t, 3H).

후처리

  1. temperatureto reflux for 4 hr
  2. extractionthe mixture was extracted with dichloromethane (3×50 mL)
  3. washthe combined organic layers were washed with water, brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationFiltration and concentration
  6. distillationdistillation

출처 및 근거

ORD 기록
ord-f1cf5457b8ef4e3383eb898f3b021a25
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08012956B2

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