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

Hydrogen Peroxide → HCID 131716835, 화합물

HRID 1085924
노트
인쇄 미리보기

반응식

HRID 1085924 반응식
[O:1]1[CH2:5][C:4](=[O:6])[N:3]=[C-:2]1.[O-]S(C(F)(F)F)(=O)=O.C([B+]CCCC)CCC.COC1C=C[C:29]([CH2:30][O:31][CH2:32][CH2:33]C=O)=CC=1.P([O-])([O-])([O-])=O.OO>C(Cl)Cl.C(N(CC)CC)C>[O:1]1[CH2:5][C:4](=[O:6])[N:3]=[C-:2]1.[CH3:29][CH2:30][O:31][CH2:32][CH3:33]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 784Hydrogen PeroxideHCID 1061PhosphateHCID 10997887Propanal, 3-[(4-methoxyphenyl)methoxy]-HCID 532495662H-1,3-oxazol-2-id-4-oneHCID 178418657HCID 178418657, 화합물

생성물 1

HCID 131716835HCID 131716835, 화합물

시약·촉매·용매 2

HCID 6344
Dichloromethane
용매
3회
HCID 8471Triethylamine용매

반응 조건

온도
0 °C

실험 절차

To a solution of 3.21 g of the oxazolidone 15 in 40 ml of methylene chloride at -78° C. was added 13.64 ml of a 1M dibutylboron triflate in methylene chloride solution and 2.6 ml of triethylamine. The reaction solution was stirred at 0° C. for 30 minutes, then it was cooled to -78° C. 3-(4-Methoxybenzyloxy)propanaldehyde (2.4 g) in 4 ml of methylene chloride was added and the reaction solution was stirred 30 minutes at -78° C. and then at RT for 1.5 hour. At the end of this time 100 ml of pH7 phosphate buffer was added, followed by addition of 30% aqueous hydrogen peroxide to the mixture at 0° C. The mixture was then extracted twice with diethyl ether and the aqueous phases were dried with sodium sulfate. The solution was concentrated under vacuum and chromatography of the residue over silica gel (2 hexanes: 1 EtOAc) provided the title compound.

후처리

  1. temperatureit was cooled to -78° C
  2. stirringthe reaction solution was stirred 30 minutes at -78° C.
  3. waitat RT for 1.5 hour
  4. extractionThe mixture was then extracted twice with diethyl ether
  5. dry with materialthe aqueous phases were dried with sodium sulfate
  6. concentrationThe solution was concentrated under vacuum and chromatography of the residue over silica gel (2 hexanes: 1 EtOAc)

출처 및 근거

ORD 기록
ord-4d13c309a9c844378dcbee9b1c0f0daf
출처 데이터셋
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05011943

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트