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1,1-Dimethylethyl 4-[[2-methoxy-5-(1-methylethyl)phenyl]methyl]-1-piperazinecarboxylate → 1-[[2-Methoxy-5-(1-methylethyl)phenyl]methyl]-piperazine

HRID 38291
ノート
印刷プレビュー

反応式

HRID 38291 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]([CH3:11])[CH3:10])=[CH:5][C:4]=1[CH2:12][N:13]1[CH2:18][CH2:17][N:16](C(OC(C)(C)C)=O)[CH2:15][CH2:14]1>C(O)(C(F)(F)F)=O.ClCCl>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]([CH3:11])[CH3:10])=[CH:5][C:4]=1[CH2:12][N:13]1[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 671315531,1-Dimethylethyl 4-[[2-methoxy-5-(1-methylethyl)phenyl]methyl]-1-piperazinecarboxylate

生成物 1

HCID 39064451-[[2-Methoxy-5-(1-methylethyl)phenyl]methyl]-piperazine収率 126.8%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 6422Trifluoroacetic acid溶媒

実験手順

A solution of the product from step (a) (1.98 g) in TFA (4 ml) and dichloromethane (2 ml) was stirred for 2 h. The solvent was removed in vacuo and the residue azeotroped with toluene. Aq. potassium carbonate was added and the mixture was extracted with dichloromethane. The organic extracts were dried (MgSO4) and evaporated in vacuo to give the sub-title compound (1.79 g).

後処理

  1. customThe solvent was removed in vacuo
  2. customthe residue azeotroped with toluene
  3. additionAq. potassium carbonate was added
  4. extractionthe mixture was extracted with dichloromethane
  5. dry with materialThe organic extracts were dried (MgSO4)
  6. customevaporated in vacuo

出典と根拠

ORDレコード
ord-cb22901767bf426b84b966e953a02f2d
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08524715B2

反応ノート

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