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Formaldehyde → Methyl 4-(2-hydroxy-5-methoxybenzyl)-1-piperazinecarbodithioate

HRID 1757532
ノート
印刷プレビュー

反応式

HRID 1757532 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.[CH3:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([OH:21])=[CH:17][CH:16]=1>C(O)C>[OH:21][C:18]1[CH:19]=[CH:20][C:15]([O:14][CH3:13])=[CH:16][C:17]=1[CH2:1][N:6]1[CH2:7][CH2:8][N:3]([C:9]([S:11][CH3:12])=[S:10])[CH2:4][CH2:5]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 712FormaldehydeHCID 90154-MethoxyphenolHCID 21278808Methyl piperazine-1-carbodithioate

生成物 1

HCID 19388436Methyl 4-(2-hydroxy-5-methoxybenzyl)-1-piperazinecarbodithioate収率 34%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To 20 ml of ethanol was 1.05 g of 37% formalin, and to the mixture was added under chilling with ice 2.29 g of methyl 1-piperazinecarbodithioate.The mixture was then stirred for 30 min. at room temperature, and, after addition of 1.24 g of 4-methoxyphenol, refluxed overnight under heating. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography. The obtained oil was crystallized from 10 ml of ethanol. The crystals were collected by filtration and subsequently washed with ethanol to give 1.06 g of the desired compound as white crystals, m.p. 112° C., yield 34%.

後処理

  1. additionto the mixture was added
  2. temperaturerefluxed overnight
  3. temperatureunder heating
  4. distillationThe solvent was distilled off under reduced pressure
  5. customthe residue was purified by silica gel column chromatography
  6. customThe obtained oil was crystallized from 10 ml of ethanol
  7. filtrationThe crystals were collected by filtration
  8. washsubsequently washed with ethanol

出典と根拠

ORDレコード
ord-ff4d30981a7a4a5692f88990382ebfac
出典データセット
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05446146

反応ノート

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