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

HCID 68698382, 화합물 → 3,5-Diethoxy-4-methoxybenzaldehyde

HRID 1990886
노트
인쇄 미리보기

반응식

HRID 1990886 반응식
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([CH2:15][OH:16])[CH:7]=[C:8]([O:12][CH2:13][CH3:14])[C:9]=1[O:10][CH3:11])[CH3:2]>C1COCC1.O=[Mn]=O>[CH2:13]([O:12][C:8]1[CH:7]=[C:6]([CH:5]=[C:4]([O:3][CH2:1][CH3:2])[C:9]=1[O:10][CH3:11])[CH:15]=[O:16])[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 68698382HCID 68698382, 화합물

생성물 1

HCID 587063513,5-Diethoxy-4-methoxybenzaldehyde수율 48%

시약·촉매·용매 2

HCID 14801Manganese dioxide촉매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of (3,5-diethoxy-4-methoxy-phenyl)-methanol (0.26 g, 1.15 mmol, 1.0 equiv) in THF (10 mL) was added activated MnO2 (1.0 g, 11.49 mmol, 10.0 equiv) and the reaction mixture stirred at rt for 4 h. Filtration through Hyflo Super Cel, concentration by evaporation under reduced pressure and purification with column chromatography on silica eluting with hexane/ethyl acetate (5:1) yielded 0.12 g (48%) of the title compound. 1H NMR (300 MHz, CDCl3): δ 1.47 (t, J=7.0 Hz, 6H), 3.94 (s, 3H), 4.14 (q, J=7.0 Hz, 4H), 7.10 (s, 2H), 9.84 (s, 1H). MS (ISP): 225.1 [M+H]+.

후처리

  1. filtrationFiltration
  2. concentrationthrough Hyflo Super Cel, concentration
  3. customby evaporation
  4. customunder reduced pressure and purification with column chromatography on silica eluting with hexane/ethyl acetate (5:1)

출처 및 근거

ORD 기록
ord-a8c4757608a04c99a51a56eabe92e75d
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07645753B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트