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Hydrochloric Acid → Ethyl 1-methyl-4-oxo-1,4-dihydroquinoline-2-carboxylate

HRID 1065110
노트
인쇄 미리보기

반응식

HRID 1065110 반응식
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9](=[O:11])[CH3:10].[O-]CC.[Na+].[C:16](OCC)(=O)[C:17]([O:19][CH2:20][CH3:21])=[O:18].[Na].Cl>C(O)C>[CH3:1][N:2]1[C:3]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:9](=[O:11])[CH:10]=[C:16]1[C:17]([O:19][CH2:20][CH3:21])=[O:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 313Hydrochloric AcidHCID 7268Diethyl OxalateHCID 2723922Sodium ethoxideHCID 5360545SodiumHCID 155795831-[2-(Methylamino)phenyl]ethan-1-one

생성물 1

HCID 13223147Ethyl 1-methyl-4-oxo-1,4-dihydroquinoline-2-carboxylate수율 70%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

149 mgs (1 mMol) of 1-(2'-methylaminophenyl)ethanone was heated under reflux with 4 mMol of sodium ethoxide and 4 mMol of diethyl oxalate in 7 ml of ethanol for 11/2 hr. The reaction mixture, which contained the sodium salt of ethyl (2-N-methylaminobenzoyl)pyruvic acid was poured into dilute hydrochloric acid and extracted with chloroform. Evaporation to dryness and boiling the residue in diethyl ether afforded, after storing at 0°-5°, 160 mgs (70%) of the title product, mp 114°-5°.

후처리

  1. extractionextracted with chloroform
  2. customEvaporation to dryness
  3. customafforded
  4. customafter storing at 0°-5°

출처 및 근거

ORD 기록
ord-f03a62cbe82644da8f8f5ad122da8033
출처 데이터셋
uspto-grants-1982_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04328341

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