Methylparaben → Benzoic acid, 4-[(1-methyl-4-piperidinyl)oxy]-, methyl ester

HRID 1626284노트

반응식

HRID 1626284 반응식
[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]([OH:8])[CH2:4][CH2:3]1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[CH3:28][O:29][C:30](=[O:38])[C:31]1[CH:36]=[CH:35][C:34](O)=[CH:33][CH:32]=1.N(C(OCC)=O)=NC(OCC)=O>C1COCC1>[CH3:28][O:29][C:30](=[O:38])[C:31]1[CH:36]=[CH:35][C:34]([O:8][CH:5]2[CH2:6][CH2:7][N:2]([CH3:1])[CH2:3][CH2:4]2)=[CH:33][CH:32]=1

참가 물질

6

실험 절차

To a solution of 1-methyl-piperidin-4-ol (6.8 g. 59 mmoles), PPh3 (triphenylphosphine, 15.5 g, 59 mmoles) and 4-hydroxy-benzoic acid methyl ester (6 g, 39 mmoles) in THF (150 ml) at 0° C., diethyl azodicarboxylate (9.5 ml, 59 mmoles) in THF (30 ml) was slowly added. The reaction mixture was allowed to warm to room temperature over a period of 24 hours. It was then evaporated and the residue redissolved in 5% aqueous citric acid (700 ml). The solution was washed with ethyl acetate (3×250 ml), made alkaline with concentrated NH4OH (pH ˜8) and then extracted with dichloromethane (3×250 ml). The combined dichloromethane extracts were washed with brine, dried and evaporated to give an oil which was purified by flash chromatography on silica gel using dichloromethane-MeOH (90:10) as eluent, to give the title compound as a yellow oil (7.4 g, 75%).

후처리

  1. customIt was then evaporated
  2. dissolutionthe residue redissolved in 5% aqueous citric acid (700 ml)
  3. washThe solution was washed with ethyl acetate (3×250 ml)
  4. extractionextracted with dichloromethane (3×250 ml)
  5. washThe combined dichloromethane extracts were washed with brine
  6. customdried
  7. customevaporated
  8. customto give an oil which
  9. customwas purified by flash chromatography on silica gel

출처 및 근거

ORD 기록
ord-17f564cde3b34ae4b57fd97b811fde87
출처 데이터셋
uspto-grants-2014_07
특허 번호
US08785448B2

반응 노트

불러오는 중…