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Hydrochloric Acid → N-(2-fluoroethyl)-N-methyloxamic acid

HRID 45307
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HRID 45307 반응식
[CH3:1]O.[OH-].[Na+].Cl.[F:6][CH2:7][CH2:8][N:9](NC)[C:10](=[O:14])[C:11]([OH:13])=[O:12]>O>[F:6][CH2:7][CH2:8][N:9]([CH3:1])[C:10](=[O:14])[C:11]([OH:13])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 14798Sodium HydroxideHCID 86661508N-(2-fluoroethyl)-N-methylaminooxamic acid

생성물 1

HCID 55301814N-(2-fluoroethyl)-N-methyloxamic acid수율 66%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a mixed solvent comprising 6 ml of methanol and 5 ml of water, there was suspended 1.56 g of N-(2-fluoroethyl)-N-methylmethoxyoxalylamide, then 3.2 g of a 15% aqueous solution of sodium hydroxide was dropwise added, with ice-cooling, to the suspension and then the mixture was stirred for one hour. Concentrated hydrochloric acid was added to the reaction system, the mixture was then extracted with ethyl acetate, the organic phase thus separated was washed with water, dried over magnesium sulfate and then the ethyl acetate was distilled off from the organic phase to thus give, as the target product, 0.94 g (yield: 66%, a solid product) of N-(2-fluoroethyl)-N-methylaminooxamic acid.

후처리

  1. temperaturecooling, to the suspension
  2. extractionthe mixture was then extracted with ethyl acetate
  3. customthe organic phase thus separated
  4. washwas washed with water
  5. dry with materialdried over magnesium sulfate
  6. distillationthe ethyl acetate was distilled off from the organic phase
  7. customto thus give, as the target product, 0.94 g (yield: 66%

출처 및 근거

ORD 기록
ord-d44f2c5488034fda8a8f1830b69e4112
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08541473B2

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