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Sodium Hydroxide → 5-[5-(2-Methoxyphenyl)[1,2,4]oxadiazol-3-yl]pentanoic acid

HRID 1443686
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반응식

HRID 1443686 반응식
[OH-].[Na+].[CH3:3][O:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]1[O:15][N:14]=[C:13]([CH2:16][CH2:17][CH2:18][CH2:19][C:20]([O:22]C)=[O:21])[N:12]=1>CO>[CH3:3][O:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]1[O:15][N:14]=[C:13]([CH2:16][CH2:17][CH2:18][CH2:19][C:20]([OH:22])=[O:21])[N:12]=1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 59167762Methyl 5-[5-(2-methoxyphenyl)[1,2,4]oxadiazol-3-yl]pentanoate

생성물 1

HCID 684879075-[5-(2-Methoxyphenyl)[1,2,4]oxadiazol-3-yl]pentanoic acid수율 72.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Add a solution of 2 N sodium hydroxide (20 mL) to a solution of methyl 5-[5-(2-methoxyphenyl)[1,2,4]oxadiazol-3-yl]pentanoate (3.4 g, 11 mmol) in methanol (50 mL) at room temperature under nitrogen and stir the mixture for 3.5 h. Remove the solvent under reduced pressure, dilute the residue with water (200 mL) and wash with diethyl ether (200 mL). Adjust the aqueous layer to pH 1 with 1 N HCl and collect the solids by vacuum filtration to afford 5-[5-(2-methoxyphenyl)[1,2,4]oxadiazol-3-yl]pentanoic acid (2.2 g, 72%): APCI MS m/z 275 [C14H16N2O4−H]−.

후처리

  1. customRemove the solvent under reduced pressure
  2. additiondilute the residue with water (200 mL)
  3. washwash with diethyl ether (200 mL)
  4. customcollect the solids
  5. filtrationby vacuum filtration

출처 및 근거

ORD 기록
ord-e6cdb4e4a89d437b84d3d08a9ba6f07c
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07662771B2

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