Methyl 3-(5-phenyl-1,3,4-oxadiazol-2-yl)propanoate → 5-Phenyl-1,3,4-oxadiazole-2-propionic acid

HRID 1787803ノート

反応式

HRID 1787803 の反応式
[C:1]1([C:7]2[O:11][C:10]([CH2:12][CH2:13][C:14]([O:16]C)=[O:15])=[N:9][N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>[OH-].[Na+].CO>[C:1]1([C:7]2[O:11][C:10]([CH2:12][CH2:13][C:14]([OH:16])=[O:15])=[N:9][N:8]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

参加物

4

反応物 1

HCID 57600262Methyl 3-(5-phenyl-1,3,4-oxadiazol-2-yl)propanoate

生成物 1

HCID 71306335-Phenyl-1,3,4-oxadiazole-2-propionic acid収率 114.6%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 14798Sodium Hydroxide溶媒

実験手順

A mixture of methyl 3-(5-phenyl-1,3,4-oxadiazol-2-yl)propanoate (600 mg, 2.0 mmol) in 1 M of aqueous NaOH (10 mL) and Methanol (10 mL) was stirred at room temperature overnight. The reaction solution was adjusted to pH 5 and extracted with ethyl acetate three times. The combined organic layers were dried, filtered and concentrated to yield the desired product (0.50 g, 83%). LCMS calculated for C11H11N2O3(M+H): 219.1; found 219.1.

後処理

  1. extractionextracted with ethyl acetate three times
  2. customThe combined organic layers were dried
  3. filtrationfiltered
  4. concentrationconcentrated

出典と根拠

ORDレコード
ord-7346673dc2d34e998c69654afd855478
出典データセット
uspto-grants-2009_03
特許番号
US07511050B2

反応ノート

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