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Water → Benzaldehyde, 4-(trifluoromethyl)-, oxime

HRID 843359
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HRID 843359 반응식
[F:1][C:2]([F:12])([F:11])[C:3]1[CH:10]=[CH:9][C:6]([CH:7]=O)=[CH:5][CH:4]=1.Cl.[NH2:14][OH:15].O.[OH-].[Na+]>C(O)C.CCOCC>[F:1][C:2]([F:12])([F:11])[C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[N:14][OH:15])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 962WaterHCID 14798Sodium HydroxideHCID 679964-(Trifluoromethyl)benzaldehydeHCID 443297Hydroxyamine hydrochloride

생성물 1

HCID 3056297Benzaldehyde, 4-(trifluoromethyl)-, oxime수율 95.5%

시약·촉매·용매 2

HCID 702Ethanol용매
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 3283
Diethyl Ether
용매

실험 절차

The first step of the process of the present invention was conducted as follows. At first, 8.79 g (50.5 mmol) of 4-trifluoromethylbenzaldehyde and 3.83 g (55.1 mmol) of hydroxylamine hydrochloride were dissolved in 12.5 ml of ethanol and 34 ml of water followed by the addition of 2.5 g of sodium hydroxide and stirring for 1 hour at room temperature. After adding ether and washing with dilute hydrochloric acid, the reaction liquid was further washed with saturated brine followed by drying with mirabilite and concentrating to obtain 9.25 g (48.2 mmol) of 4-trifluoromethylbenzaldehyde oxime (yield: 95.5%).

후처리

  1. washwashing with dilute hydrochloric acid
  2. customthe reaction liquid
  3. washwas further washed with saturated brine
  4. dry with materialby drying with mirabilite
  5. concentrationconcentrating

출처 및 근거

ORD 기록
ord-155f64241f6e4c2ebd5c431fcaf9a6c9
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06376712B2

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