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

HRID 1015612
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HRID 1015612 반응식
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]
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참가 물질

4

반응물 2

HCID 168937Lithium hydroxide, monohydrateHCID 700562Methyl 3-amino-5-phenylthiophene-2-carboxylate

생성물 1

HCID 198432823-Amino-5-phenylthiophene-2-carboxylic acid수율 88.2%

시약·촉매·용매 1

HCID 21892291Methanol tetrahydrofuran water용매

반응 조건

온도
85 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-97197f080c6d4113b0446660de63255a
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07985769B2

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