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Lithium Hydroxide → 2-(3-(3-Hexylquinoline-8-carboxamido)phenoxy)acetic acid

HRID 472793
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HRID 472793 반응식
[OH-].[Li+].[CH2:3]([C:9]1[CH:10]=[N:11][C:12]2[C:17]([CH:18]=1)=[CH:16][CH:15]=[CH:14][C:13]=2[C:19]([NH:21][C:22]1[CH:23]=[C:24]([CH:33]=[CH:34][CH:35]=1)[O:25][CH2:26][C:27]([O:29]C(C)C)=[O:28])=[O:20])[CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]>O>[CH2:3]([C:9]1[CH:10]=[N:11][C:12]2[C:17]([CH:18]=1)=[CH:16][CH:15]=[CH:14][C:13]=2[C:19]([NH:21][C:22]1[CH:23]=[C:24]([CH:33]=[CH:34][CH:35]=1)[O:25][CH2:26][C:27]([OH:29])=[O:28])=[O:20])[CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 3939Lithium HydroxideHCID 66660805Isopropyl 2-(3-(3-hexylquinoline-8-carboxamido)phenoxy)acetate

생성물 1

HCID 565964142-(3-(3-Hexylquinoline-8-carboxamido)phenoxy)acetic acid수율 93%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Aqueous 2 N lithium hydroxide (0.7 mL, 1.4 mmol) and water (0.7 mL) were added to a solution of isopropyl 2-(3-(3-hexylquinoline-8-carboxamido)phenoxy)acetate (210 mg, 0.47 mmol) in THE (5.0 mL) and the solution was stirred at room temperature. After 20 h, the THF was removed in vacuo. The residual aqueous phase was adjusted to pH 4-5 with 1 N aqueous HCl and extracted with EtOAc (3×). The combined organic phase was dried (MgSO4), filtered and concentrated in vacuo to afford 177 mg (93%) of the title compound.

후처리

  1. customthe THF was removed in vacuo
  2. extractionextracted with EtOAc (3×)
  3. dry with materialThe combined organic phase was dried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-b996075c65e44fd59926d12df1db2e38
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08633220B2

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