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

1-(6-Methoxy-benzofuran-3-yl)-ethane-1,2-diol → 6-Methoxybenzofuran-3-carbaldehyde

HRID 273336
노트
인쇄 미리보기

반응식

HRID 273336 반응식
[CH3:1][O:2][C:3]1[CH:15]=[CH:14][C:6]2[C:7]([CH:10]([OH:13])CO)=[CH:8][O:9][C:5]=2[CH:4]=1>C1COCC1.O>[CH3:1][O:2][C:3]1[CH:15]=[CH:14][C:6]2[C:7]([CH:10]=[O:13])=[CH:8][O:9][C:5]=2[CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 691973081-(6-Methoxy-benzofuran-3-yl)-ethane-1,2-diol

생성물 1

HCID 824109866-Methoxybenzofuran-3-carbaldehyde수율 73%

시약·촉매·용매 2

HCID 962Water용매2회HCID 8028Tetrahydrofuran용매

실험 절차

NaIO4 (0.204 g, 1.12 mmol) was added to 1-(6-methoxy-benzofuran-3-yl)-ethane-1,2-diol (0.180 g, 1.196 mmol) in THF (50 mL) and water (1 mL) with stirring. The mixture was stirred overnight at room temperature under N2. Water (10 mL) was added, and the mixture was concentrated to half its volume and extracted with EtOAc. The organic layer was washed with brine and water, dried over anhyd. MgSO4, and evaporated to give a residue, which was purified on a silica gel column eluting with EtOAc/hexane (1:10) to give 6-methoxybenzofuran-3-carbaldehyde (0.110 g, 73%).

후처리

  1. stirringThe mixture was stirred overnight at room temperature under N2
  2. concentrationthe mixture was concentrated to half its volume
  3. extractionextracted with EtOAc
  4. washThe organic layer was washed with brine and water
  5. customdried over anhyd
  6. customMgSO4, and evaporated
  7. customto give a residue, which
  8. customwas purified on a silica gel column
  9. washeluting with EtOAc/hexane (1:10)

출처 및 근거

ORD 기록
ord-48aeedf470cd4b08826f5be8112c6084
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07456289B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트