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Potassium Hydroxide → 7-[4-(4-Morpholinyl)phenyl]-1-benzothiophene-2-carboxylic acid

HRID 2179578
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HRID 2179578 반응식
[N:1]1([C:7]2[CH:12]=[CH:11][C:10]([C:13]3[C:21]4[S:20][C:19]([C:22]([O:24]C)=[O:23])=[CH:18][C:17]=4[CH:16]=[CH:15][CH:14]=3)=[CH:9][CH:8]=2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[OH-].[K+]>CO>[N:1]1([C:7]2[CH:12]=[CH:11][C:10]([C:13]3[C:21]4[S:20][C:19]([C:22]([OH:24])=[O:23])=[CH:18][C:17]=4[CH:16]=[CH:15][CH:14]=3)=[CH:9][CH:8]=2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1
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참가 물질

4

반응물 2

HCID 14797Potassium HydroxideHCID 58485644Methyl 7-[4-(4-morpholinyl)phenyl]-1-benzothiophene-2-carboxylate

생성물 1

HCID 179826497-[4-(4-Morpholinyl)phenyl]-1-benzothiophene-2-carboxylic acid수율 111.7%

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
50 °C

실험 절차

A solution of 330 mg (0.77 mmol) of methyl 7-[4-(4-morpholinyl)phenyl]-1-benzothiophene-2-carboxylate (Example 19A) in 6 ml of a 1:1 mixture of methanol and 2N potassium hydroxide solution is stirred at room temperature for 2 h and at 50° C. for 1 h. The reaction mixture is concentrated in vacuo and, after addition of water, acidified with conc. hydrochloric acid. The resulting precipitate is filtered off with suction, washed twice with water and dried under high vacuum. 292 mg of crude product are obtained and reacted without further purification.

후처리

  1. concentrationThe reaction mixture is concentrated in vacuo
  2. additionafter addition of water
  3. filtrationThe resulting precipitate is filtered off with suction
  4. washwashed twice with water
  5. customdried under high vacuum

출처 및 근거

ORD 기록
ord-cea1042eacfe4ac5a52aa44cd093ba0d
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09067931B2

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