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

Triphenylphosphine → Tert-butyl 4-(2-(4-bromo-2-(trifluoromethyl)phenoxy)ethyl)piperidine-1-carboxylate

HRID 517937
노트
인쇄 미리보기

반응식

HRID 517937 반응식
CC(OC(/N=N/C(OC(C)C)=O)=O)C.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Br:34][C:35]1[CH:40]=[CH:39][C:38]([OH:41])=[C:37]([C:42]([F:45])([F:44])[F:43])[CH:36]=1.O[CH2:47][CH2:48][CH:49]1[CH2:54][CH2:53][N:52]([C:55]([O:57][C:58]([CH3:61])([CH3:60])[CH3:59])=[O:56])[CH2:51][CH2:50]1>C(Cl)Cl>[Br:34][C:35]1[CH:40]=[CH:39][C:38]([O:41][CH2:47][CH2:48][CH:49]2[CH2:50][CH2:51][N:52]([C:55]([O:57][C:58]([CH3:59])([CH3:61])[CH3:60])=[O:56])[CH2:53][CH2:54]2)=[C:37]([C:42]([F:43])([F:44])[F:45])[CH:36]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 11776TriphenylphosphineHCID 142784o-Cresol, 4-bromo-alpha,alpha,alpha-trifluoro-HCID 8541401-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 5363146Diisopropyl azodicarboxylate

생성물 1

HCID 67294273Tert-butyl 4-(2-(4-bromo-2-(trifluoromethyl)phenoxy)ethyl)piperidine-1-carboxylate

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

DIAD (33.5 g) was added dropwise to the solution of triphenylphosphine (43.5 g), 4-bromo-2-trifluoromethylphenol (40 g) and tert-butyl 4-(2-hydroxyethyl)-piperidine-1-carboxylate (31.7 g) in DCM (200 ml) at 0° C. during 15 minutes. The mixture was then stirred at room temperature for 20 hours. After removal of DCM under reduced pressure, to the residue was added ether (100 ml) and heptane (300 ml), solid was then filtered off. Filtrate was then washed with 1M sodium hydroxide (100 ml×3). Organic layer dried over sodium sulphate, solvent removed under vacuum, residue was then columned on silica gel using heptane:EtOAc (5:1) as eluant to give tert-butyl 4-(2-(4-bromo-2-(trifluoromethyl)phenoxy)ethyl)piperidine-1-carboxylate as a colorless oil as product (61.3 g).

후처리

  1. customAfter removal of DCM under reduced pressure
  2. additionto the residue was added ether (100 ml) and heptane (300 ml), solid
  3. filtrationwas then filtered off
  4. washFiltrate was then washed with 1M sodium hydroxide (100 ml×3)
  5. dry with materialOrganic layer dried over sodium sulphate, solvent
  6. customremoved under vacuum, residue

출처 및 근거

ORD 기록
ord-397246aa07b34753bc7c02ee9f38aeec
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115126B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트