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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methyl (4-ethylpiperazin-1-YL)acetate → (4-ethylpiperazin-1-yl)acetic acid

HRID 64061
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HRID 64061 반응식
[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]
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참가 물질

3

반응물 1

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

생성물 1

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

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

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).

후처리

  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)

출처 및 근거

ORD 기록
ord-4544f572bade4515a070798b53bfd761
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09447091B2

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