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Methyl (4-ethylpiperazin-1-YL)acetate → (4-ethylpiperazin-1-yl)acetic acid

HRID 64061
ノート
印刷プレビュー

反応式

HRID 64061 の反応式
[CH2:1]([N:3]1[CH2:8][CH2:7][N:6]([CH2:9][C:10]([O:12]C)=[O:11])[CH2:5][CH2:4]1)[CH3:2]>Cl>[CH2:1]([N:3]1[CH2:8][CH2:7][N:6]([CH2:9][C:10]([OH:12])=[O:11])[CH2:5][CH2:4]1)[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 22199026Methyl (4-ethylpiperazin-1-YL)acetate

生成物 1

HCID 3163246(4-ethylpiperazin-1-yl)acetic acid収率 54.5%

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

The solution of methyl 2-(4-ethylpiperazin-1-yl)acetate (1.3 g, 6.50 mmol, 1.0 eq) in 8 N HCl was stirred at 95° C. for 16 h and concentrated on vacuum pump. The mixture was quenched with sodium bicarbonate solution and extracted with ethyl acetate (3×150 ml). The combined organic layer was washed with water, brine and dried over sodium sulphate. The solvent was distilled off to give the product in 54.5% yield (0.6 g). LC-MS (ESI): Calculated mass: 158.0; Observed mass: 159.1 [M+H]+ (rt: 0.102 min).

後処理

  1. concentrationconcentrated on vacuum pump
  2. customThe mixture was quenched with sodium bicarbonate solution
  3. extractionextracted with ethyl acetate (3×150 ml)
  4. washThe combined organic layer was washed with water, brine
  5. dry with materialdried over sodium sulphate
  6. distillationThe solvent was distilled off
  7. customto give the product in 54.5% yield (0.6 g)
  8. custom159.1 [M+H]+ (rt: 0.102 min)

出典と根拠

ORDレコード
ord-4544f572bade4515a070798b53bfd761
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09447091B2

反応ノート

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