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

Methanol → 4-(3-Amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromide

HRID 2271450
노트
인쇄 미리보기

반응식

HRID 2271450 반응식
Br.[NH2:2][C:3]1[C:4]([O:17]C)=[C:5]([C:9]2[CH:10]=[C:11]([C:14]([OH:16])=[O:15])[S:12][CH:13]=2)[CH:6]=[CH:7][CH:8]=1.B(Br)(Br)[Br:20].CO>ClCCl>[BrH:20].[NH2:2][C:3]1[C:4]([OH:17])=[C:5]([C:9]2[CH:10]=[C:11]([C:14]([OH:16])=[O:15])[S:12][CH:13]=2)[CH:6]=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 25134Boron tribromideHCID 574838484-(3-Amino-2-methoxy-phenyl)-thiophene-2-carboxylic acid hydrobromide

생성물 1

HCID 574838464-(3-Amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromide수율 17.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

4-(3-Amino-2-methoxy-phenyl)-thiophene-2-carboxylic acid hydrobromide 19b (360 mg, 1.45 mmol) was dissolved in 5 mL of dichloromethane followed by dropwise addition of boron tribromide (2.8 mL, 5.6 mmol). The reaction mixture was reacted at room temperature for 4.5 hours. The reaction mixture was added with 5 mL of methanol and concentrated under reduced pressure. The residue was diluted with 10 mL of ethyl acetate and stirred for 0.5 hours. The mixture was filtered and the filter cake was dried to obtain the title compound 4-(3-amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromide 19c (80 mg, yield 17.5%) as a grey solid.

후처리

  1. customThe reaction mixture was reacted at room temperature for 4.5 hours
  2. concentrationconcentrated under reduced pressure
  3. additionThe residue was diluted with 10 mL of ethyl acetate
  4. filtrationThe mixture was filtered
  5. customthe filter cake was dried

출처 및 근거

ORD 기록
ord-b51b34059dbc4dc5a7f1257de5b209e4
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09120762B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트