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Sodium Hydroxide → 3-(Quinolin-8-yl)benzoic acid

HRID 1626756
ノート
印刷プレビュー

反応式

HRID 1626756 の反応式
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[C:11]2[CH:12]=[C:13]([CH:18]=[CH:19][CH:20]=2)[C:14]([O:16]C)=[O:15])[CH:4]=[CH:3][CH:2]=1.[OH-].[Na+]>C1COCC1>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[C:11]2[CH:12]=[C:13]([CH:18]=[CH:19][CH:20]=2)[C:14]([OH:16])=[O:15])[CH:4]=[CH:3][CH:2]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 4189037HCID 4189037、化合物

生成物 1

HCID 41889673-(Quinolin-8-yl)benzoic acid収率 92%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
60 °C

実験手順

820 mg (3.11 mmol) of methyl 3-(quinolin-8-yl)benzoate was dissolved in 8.2 mL of THF, and a 1N aqueous sodium hydroxide solution (4.7 mL) was added thereto at room temperature. The mixture was stirred at 60° C. for 1.5 hours. Thereafter, the organic solvent was distilled off under reduced pressure, H2O was added to the resulting residue, and then dissolution was conducted. Thereafter, 1N hydrochloric acid was added to the resultant at 0° C., and the pH was adjusted to 4. The precipitated solids were collected by filtration and dried, thereby giving 711 mg of 3-(quinolin-8-yl)benzoic acid (yield: 92%).

後処理

  1. customat room temperature
  2. distillationThereafter, the organic solvent was distilled off under reduced pressure, H2O
  3. additionwas added to the resulting residue
  4. dissolutiondissolution
  5. additionThereafter, 1N hydrochloric acid was added to the resultant at 0° C.
  6. filtrationThe precipitated solids were collected by filtration
  7. customdried

出典と根拠

ORDレコード
ord-a11fef8394b5422ba726bbd86266bb83
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08785473B2

反応ノート

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