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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydroxyamine hydrochloride → 4-(Trifluoromethyl)picolinamide

HRID 1880717
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HRID 1880717 반응식
C(=O)(O)[O-:2].[Na+].Cl.NO.[C:9]([C:11]1[CH:16]=[C:15]([C:17]([F:20])([F:19])[F:18])[CH:14]=[CH:13][N:12]=1)#[N:10]>C(O)C>[F:19][C:17]([F:20])([F:18])[C:15]1[CH:14]=[CH:13][N:12]=[C:11]([C:9]([NH2:10])=[O:2])[CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 443297Hydroxyamine hydrochlorideHCID 516892Sodium BicarbonateHCID 203104534-(Trifluoromethyl)pyridine-2-carbonitrile

생성물 1

HCID 538130744-(Trifluoromethyl)picolinamide수율 75.4%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To 72 ml of ethanol were added 6.18 g of sodium bicarbonate and 5.11 g of hydroxylamine hydrochloride, and the mixture was heated to reflux for 45 minutes. After allowing to cool, 6 g of 2-cyano-4-trifluoromethylpyridine was added at 0° C., and the mixture was stirred, and concentrated. To the residue was added water, the resultant solution was extracted with ethyl acetate three times, and the organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography to obtain 5 g of 4-trifluoromethylpyridine-2-carboxamide=oxime.

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 45 minutes
  3. temperatureto cool
  4. concentrationconcentrated
  5. additionTo the residue was added water
  6. extractionthe resultant solution was extracted with ethyl acetate three times
  7. washwashed with an aqueous saturated sodium chloride solution
  8. dry with materialdried with anhydrous magnesium sulfate
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-72a8fdce4e554ebabeb163a4bdeaa872
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318776B2

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