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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Potassium Hydroxide → 2,2'-(Hex-5-ynylazanediyl)diacetic acid

HRID 1622063
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반응식

HRID 1622063 반응식
[CH2:1]([N:7]([CH2:13][C:14]([O:16]C)=[O:15])[CH2:8][C:9]([O:11]C)=[O:10])[CH2:2][CH2:3][CH2:4][C:5]#[CH:6].[OH-].[K+]>C1COCC1>[CH2:1]([N:7]([CH2:13][C:14]([OH:16])=[O:15])[CH2:8][C:9]([OH:11])=[O:10])[CH2:2][CH2:3][CH2:4][C:5]#[CH:6]
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참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 87118843HCID 87118843, 화합물

생성물 1

HCID 871187222,2'-(Hex-5-ynylazanediyl)diacetic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To the obtained approximately 1.4 g dimethyl 2,2′-(hex-5-ynylazanediyl)diacetate was added 20 mL THF and 20 mL of 2 M KOH. The mixture was stirred overnight and monitored by TLC. The organic layer was separated, and the aqueous layer was quenched by addition of 20 mL of 2 M HCl. The solvent (H2O) was removed by rotary evaporation, and the resulting solid was dissolved into acetonitrile (ACN). The insoluble KCl salt was filtered, and the filtrate was concentrated by rotary evaporation. The final product of free acid was obtained as a greasy, transparent oil. Yield was quantitative. ESI-MS: [M+H]+ m/z 214.1.

후처리

  1. customThe organic layer was separated
  2. customthe aqueous layer was quenched by addition of 20 mL of 2 M HCl
  3. customThe solvent (H2O) was removed by rotary evaporation
  4. dissolutionthe resulting solid was dissolved into acetonitrile (ACN)
  5. filtrationThe insoluble KCl salt was filtered
  6. concentrationthe filtrate was concentrated by rotary evaporation

출처 및 근거

ORD 기록
ord-349d142eb7e44a1580f1c236d3f0d03c
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08778626B2

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