홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

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

HRID 1012704
노트
인쇄 미리보기

반응식

HRID 1012704 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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

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-e77c683147f1468bab587281d618ecd8
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07977485B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트