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

Hydrochloric Acid → 2-(3-Methoxyquinolin-6-yl)propanoic acid hydrochloride

HRID 219207
노트
인쇄 미리보기

반응식

HRID 219207 반응식
[CH3:1][O:2][C:3]1[CH:4]=[N:5][C:6]2[C:11]([CH:12]=1)=[CH:10][C:9]([CH:13]([CH3:21])[C:14]([O:16]C(C)(C)C)=[O:15])=[CH:8][CH:7]=2.[ClH:22]>CCOC(C)=O>[ClH:22].[CH3:1][O:2][C:3]1[CH:4]=[N:5][C:6]2[C:11]([CH:12]=1)=[CH:10][C:9]([CH:13]([CH3:21])[C:14]([OH:16])=[O:15])=[CH:8][CH:7]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 57691376Tert-butyl 2-(3-methoxyquinolin-6-yl)propanoate

생성물 1

HCID 675035432-(3-Methoxyquinolin-6-yl)propanoic acid hydrochloride수율 99.9%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

Tert-butyl 2-(3-methoxyquinolin-6-yl)propanoate (0.865 g, 3.01 mmol) was dissolved in EtOAc (0.2M, 15 mL), and HCl (g) (0.0915 ml, 3.01 mmol) was bubbled through the solution for approximately 5 minutes. The reaction vessel was sealed and the reaction was stirred at room temperature for 1.5 h until completion. The reaction mixture was concentrated in vacuo to yield 2-(3-methoxyquinolin-6-yl)propanoic acid hydrochloride (0.805 g, 99.9% yield) as an orange solid.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customThe reaction vessel was sealed
  2. concentrationThe reaction mixture was concentrated in vacuo

출처 및 근거

ORD 기록
ord-ac6c1c5e61404f67a09478f5cb66046a
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08198448B2

반응 노트

불러오는 중…