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

Methyl iodide → Ammonium, trimethyl(4-phenylbutyl)-, iodide

HRID 2371528
노트
인쇄 미리보기

반응식

HRID 2371528 반응식
[CH3:1][N:2]([CH2:4][CH2:5][CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[CH3:3].[CH3:14][I:15]>CO>[I-:15].[CH3:1][N+:2]([CH2:4][CH2:5][CH2:6][CH2:7][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)([CH3:14])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6328Methyl iodideHCID 13546746N,N-dimethyl-4-phenylbutylamine

생성물 1

HCID 43505Ammonium, trimethyl(4-phenylbutyl)-, iodide

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 287 mg of N,N-dimethyl-4-phenylbutylamine in 3 ml of absolute methanol, 505 μl of methyl iodide was added at a room temperature with stirring, and the mixture was stirred at a room temperature for 6.5 hours. The reaction mixture was concentrated under a reduced pressure, and after adding ethyl acetate allowed to stand for formation of crystal. The crystal was filtered, washed with ethyl acetate, and dried under a reduced pressure to obtain 439 mg of the title compound as a colorless crystal.

후처리

  1. stirringthe mixture was stirred at a room temperature for 6.5 hours
  2. concentrationThe reaction mixture was concentrated under a reduced pressure
  3. additionafter adding ethyl acetate
  4. filtrationThe crystal was filtered
  5. washwashed with ethyl acetate
  6. customdried under a reduced pressure

출처 및 근거

ORD 기록
ord-964d41e7070c4735a4c768d94607c276
출처 데이터셋
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05093370

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트