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Potassium Carbonate → HCID 178488708, 화합물

HRID 1082084
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HRID 1082084 반응식
Cl.[C:2]([NH2:5])(=[NH:4])[CH3:3].[CH3:6][O:7][C:8]1[CH:21]=[CH:20][C:11]([C:12]([CH2:14][C:15](OCC)=[O:16])=O)=[CH:10][CH:9]=1.C(=O)([O-])[O-].[K+].[K+]>C(O)C>[OH:16][C:15]1[CH:14]=[C:12]([C:11]2[CH:10]=[CH:9][C:8]([O:7][CH3:6])=[CH:21][CH:20]=2)[N:5]=[C:2]([CH3:3])[N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 67170Acetamidine monohydrochlorideHCID 76150Benzenepropanoic acid, 4-methoxy-beta-oxo-, ethyl ester

생성물 1

HCID 178488708HCID 178488708, 화합물수율 25.5%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

1.89 g of acetamidine hydrochloride and 4.44 g of etyl paramethoxybenzoylacetate were dissolved in 40 ml of ethanol. After addition of 5.52 g of potassium carbonate, the solution was refluxed with stirring for 8 hours, and then evaporated in vacuo. 5 g of sodium hydroxide was dissolved in 30 ml of water and this was added to the evaporated residue. Add ether, then extract, the aqueous layer was neutralized with acetic acid. The resulting precipitations were filtered off, washed with water and dried. Then 1.1 g of crystals were obtained. Melting point is 270° to 272° C.

후처리

  1. temperaturethe solution was refluxed
  2. customevaporated in vacuo
  3. dissolution5 g of sodium hydroxide was dissolved in 30 ml of water
  4. additionthis was added to the evaporated residue
  5. extractionAdd ether, then extract
  6. customThe resulting precipitations
  7. filtrationwere filtered off
  8. washwashed with water
  9. customdried

출처 및 근거

ORD 기록
ord-059d149148604995bdcb91bd237221cd
출처 데이터셋
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05589477

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