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Potassium Carbonate → HCID 178488708、化合物

HRID 1082084
ノート
印刷プレビュー

反応式

HRID 1082084 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 178488708HCID 178488708、化合物収率 25.5%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-059d149148604995bdcb91bd237221cd
出典データセット
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05589477

反応ノート

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