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

Benzyl(methoxymethyl)((trimethylsilyl)methyl)amine → HCID 86679676, 화합물

HRID 577750
노트
인쇄 미리보기

반응식

HRID 577750 반응식
[CH2:1]([N:8]([CH2:12][Si](C)(C)C)[CH2:9]OC)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[F:17][CH:18]([F:24])/[CH:19]=[CH:20]/[N+:21]([O-:23])=[O:22]>C(Cl)Cl.C(O)(C(F)(F)F)=O>[CH2:1]([N:8]1[CH2:12][C@@H:20]([N+:21]([O-:23])=[O:22])[C@H:19]([CH:18]([F:24])[F:17])[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 353442Benzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 86679677(1E)-3,3-difluoro-1-nitroprop-1-ene

생성물 1

HCID 86679676HCID 86679676, 화합물수율 48,780.801%

시약·촉매·용매 2

HCID 6422Trifluoroacetic acid촉매HCID 6344Dichloromethane용매

실험 절차

To a solution of N-benzyl-1-methoxy-N-((trimethylsilyl)methyl)methanamine (56.6 g, 0.24 mol) in dry CH2Cl2 (160 ml) was added (E)-3,3-difluoro-1-nitroprop-1-ene (25 g, 0.2 mmol) and a few drops of TFA at 0° C. The resulting mixture was stirred at rt overnight. The mixture was concentrated and purified by flash column chromatography (petroleum ether:EtOAc=100:1 to 25:1) to give the title compound (25 g, 49% yield) as a yellow oil.

후처리

  1. concentrationThe mixture was concentrated
  2. custompurified by flash column chromatography (petroleum ether:EtOAc=100:1 to 25:1)

출처 및 근거

ORD 기록
ord-6835ac586640405882d15af12bec5e0f
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09040547B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트