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Lithium hydroxide, monohydrate → 3-Amino-5-phenylthiophene-2-carboxylic acid

HRID 2193896
ノート
印刷プレビュー

反応式

HRID 2193896 の反応式
C[O:2][C:3]([C:5]1[S:6][C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:8][C:9]=1[NH2:10])=[O:4].O[Li].O>C1COCC1.CO.O>[NH2:10][C:9]1[CH:8]=[C:7]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[S:6][C:5]=1[C:3]([OH:4])=[O:2]
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 168937Lithium hydroxide, monohydrateHCID 700562Methyl 3-amino-5-phenylthiophene-2-carboxylate

生成物 1

HCID 198432823-Amino-5-phenylthiophene-2-carboxylic acid収率 88.2%

試薬・触媒・溶媒 1

HCID 21892291Methanol tetrahydrofuran water溶媒

反応条件

温度
85 °C

実験手順

To a suspension of 3-Amino-5-phenyl-thiophene-2-carboxylic acid methyl ester (5 g, 21.459 mmol) in a mixture of THF:MeOH:H2O (3:2:1, 75 mL), 1N aqueous solution of LiOH.H2O (64 mL, 64.378 mmol) was added. The reaction mixture was stirred at 85° C. (external temperature) for 4 h. Solvents were removed under reduced pressure and the residue was partitioned between water and ethyl acetate. The water layer was separated and acidified with 1N HCl solution and then ethyl acetate was added to it. The organic phase was separated, dried (Na2SO4) and concentrated to obtain 3-Amino-5-phenyl-thiophene-2-carboxylic acid (4.15 g, 88%) as a yellowish solid. 1H NMR (DMSO-D6, 400 MHz): 7.59 (d, 2H), 7.40 (m, 3H), 6.92 (s, 1H).

後処理

  1. additionwas added
  2. customSolvents were removed under reduced pressure
  3. customthe residue was partitioned between water and ethyl acetate
  4. customThe water layer was separated
  5. additionethyl acetate was added to it
  6. customThe organic phase was separated
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-d6692a118d48429bba350130e7d727f3
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08329924B2

反応ノート

読み込み中…

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