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

Lithium Hydroxide → 2-Methoxy-4-(3-methyl-pyrazol-1-yl)-benzoic Acid

HRID 1635882
노트
인쇄 미리보기

반응식

HRID 1635882 반응식
[CH3:1][O:2][C:3]1[CH:12]=[C:11]([N:13]2[CH:17]=[CH:16][C:15]([CH3:18])=[N:14]2)[CH:10]=[CH:9][C:4]=1[C:5]([O:7]C)=[O:6].[OH-].[Li+]>O1CCCC1>[CH3:1][O:2][C:3]1[CH:12]=[C:11]([N:13]2[CH:17]=[CH:16][C:15]([CH3:18])=[N:14]2)[CH:10]=[CH:9][C:4]=1[C:5]([OH:7])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 3939Lithium HydroxideHCID 544211052-Methoxy4-(3-methyl-pyrazol-1-yl)-benzoic acid, methyl ester

생성물 1

HCID 226054612-Methoxy-4-(3-methyl-pyrazol-1-yl)-benzoic Acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A solution of 2-methoxy-4-(3-methyl-pyrazol-1-yl)-benzoic acid methyl ester (0.5 g) from Example 105 in tetrahydrofuran (2.5 ml) was treated with 1 N lithium hydroxide (2.13 ml) at room temperature. After 14 hours the solvent was removed in vacuo and the title compound precipitated by the addition at 0° C. of 1N hydrochloric acid. After drying under vacuum 0.42 g of the title compound was obtained as a solid. MS, m/z: 232 (M)+.

후처리

  1. customAfter 14 hours the solvent was removed in vacuo
  2. customthe title compound precipitated by the addition at 0° C. of 1N hydrochloric acid
  3. dry with materialAfter drying under vacuum 0.42 g of the title compound
  4. customwas obtained as a solid

출처 및 근거

ORD 기록
ord-bcaf02d28ec04c93a83aa3ecfd81e942
출처 데이터셋
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06511974B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트