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

1,3,4-Trimethylpyridin-1-ium iodide → 2-Benzyl-1,3,4-trimethyl-1,2-dihydropyridine

HRID 1707599
노트
인쇄 미리보기

반응식

HRID 1707599 반응식
[CH2:1]([Mg]Cl)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[I-].[CH3:11][N+:12]1[CH:17]=[CH:16][C:15]([CH3:18])=[C:14]([CH3:19])[CH:13]=1>C1COCC1>[CH2:1]([CH:13]1[C:14]([CH3:19])=[C:15]([CH3:18])[CH:16]=[CH:17][N:12]1[CH3:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 125431661,3,4-Trimethylpyridin-1-ium iodideHCID 178418336HCID 178418336, 화합물

생성물 1

HCID 157330592-Benzyl-1,3,4-trimethyl-1,2-dihydropyridine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 3.02M of benzylmagnesium chloride (2M solution) in THF was added portionwise 300 g (20 g portions) of 1,3,4-trimethylpyridinium iodide. The reaction mixture was stirred at room temperature for 18 hrs. The THF was evaporated at reduced pressure, and the resulting residue was poured into iced saturated NH4Cl. The mixture was extracted with ether and the ether solution washed with additional saturated NH4Cl. The ether solution was dried over magnesium sulfate and evaporated to dryness at reduced pressure to afford 338 g of crude 2-benzyl-1,3,4-trimethyl-1,2-dihydropyridine.

후처리

  1. customThe THF was evaporated at reduced pressure
  2. additionthe resulting residue was poured into iced saturated NH4Cl
  3. extractionThe mixture was extracted with ether
  4. washthe ether solution washed with additional saturated NH4Cl
  5. dry with materialThe ether solution was dried over magnesium sulfate
  6. customevaporated to dryness at reduced pressure

출처 및 근거

ORD 기록
ord-8af43e54297642a996d015e772d2fe70
출처 데이터셋
uspto-grants-1994_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05354758

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트