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

3-Ethoxy-4-methylisoxazole-5-carboxylic acid → HCID 178431796, 화합물

HRID 1532019
노트
인쇄 미리보기

반응식

HRID 1532019 반응식
C([O:3][C:4]1[C:8]([CH3:9])=[C:7]([C:10]([OH:12])=[O:11])[O:6][N:5]=1)C>Br>[OH:3][C:4]1[C:8]([CH3:9])=[C:7]([C:10]([OH:12])=[O:11])[O:6][N:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 106787593-Ethoxy-4-methylisoxazole-5-carboxylic acid

생성물 1

HCID 178431796HCID 178431796, 화합물수율 24%

시약·촉매·용매 1

HCID 260Hydrogen Bromide용매

실험 절차

3-Ethoxy-4-methylisoxazole-5-carboxylic acid (15 g, 88 mmol) and 47% HBr (aq) (150 mL) was boiled under reflux for 6 h. The solution was cooled and crystalline title compound was collected by filtration (8.7 g, 69%): mp 257-259° C. The acidic filtrate was added water (100 mL), and extracted with diethyl ether (6×400 mL). The organic extracts were washed with brine (100 mL), dried (MgSO4) and concentrated in vacuo to give crude title compound (3.0 g, 24%). Overall yield of 93%. A mixture of the two crops were used in the next step.

후처리

  1. temperatureunder reflux for 6 h
  2. temperatureThe solution was cooled
  3. filtrationcrystalline title compound was collected by filtration (8.7 g, 69%)
  4. additionThe acidic filtrate was added water (100 mL)
  5. extractionextracted with diethyl ether (6×400 mL)
  6. washThe organic extracts were washed with brine (100 mL)
  7. dry with materialdried (MgSO4)
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-16807d7db65f49948185baaab329c411
출처 데이터셋
uspto-grants-2001_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06200999B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트