Formaldehyde → Methyl 4-(6-propyloxycarbonyl-2,3,4-trihydroxybenzyl)-1-piperazinecarbodithioate

HRID 1757535

反応式

HRID 1757535 の反応式
[CH2:1]=O.[N:3]1([C:9]([S:11][CH3:12])=[S:10])[CH2:8][CH2:7][NH:6][CH2:5][CH2:4]1.[C:13]([O:24][CH2:25][CH2:26][CH3:27])(=[O:23])[C:14]1[CH:22]=[C:20]([OH:21])[C:18]([OH:19])=[C:16]([OH:17])[CH:15]=1>C(O)C>[CH2:25]([O:24][C:13]([C:14]1[C:15]([CH2:1][N:6]2[CH2:7][CH2:8][N:3]([C:9]([S:11][CH3:12])=[S:10])[CH2:4][CH2:5]2)=[C:16]([OH:17])[C:18]([OH:19])=[C:20]([OH:21])[CH:22]=1)=[O:23])[CH2:26][CH3:27]

参加物

5

実験手順

In 10 ml of ethanol was dissolved 0.86 g (10 mmol.) of 35% formalin. To thesolution placed in an ice bath was further added a solution of 1.94 g (10 mmol., purity 90.7%) of methyl 1-piperazinecarbodithioate in 4 ml of ethanol. The resulting mixture was then stirred for 30 min. at room temperature. To the mixture placed in an ice bath was dropwise added a solution of 2.12 g (10 mmol.) of propyl gallate in 4 ml of ethanol. The mixture was stirred overnight at room temperature and subsequently refluxed under heating for 4 hours. The mixture was cooled to room temperature. Precipitated crystals were collected by filtration and washedwith ethanol to give 1.848 g of the desired compound as a grayish powder, m.p. 142°-144° C. (decomp.), yield 31.3%.

後処理

  1. customTo thesolution placed in an ice bath
  2. customTo the mixture placed in an ice bath
  3. stirringThe mixture was stirred overnight at room temperature
  4. temperaturesubsequently refluxed
  5. temperatureunder heating for 4 hours
  6. temperatureThe mixture was cooled to room temperature
  7. customPrecipitated crystals
  8. filtrationwere collected by filtration and washedwith ethanol

出典と根拠

ORDレコード
ord-add8c06a27be4b73877e44f6eb09ab5a
出典データセット
uspto-grants-1995_08
特許番号
US05446146

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