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

Sodium Cyanide → 2-{1-Azabicyclo[2.2.2]octan-4-yl}acetonitrile

HRID 1641001
노트
인쇄 미리보기

반응식

HRID 1641001 반응식
[N:1]12[CH2:8][CH2:7][C:4]([CH2:9][C:10](Cl)=O)([CH2:5][CH2:6]1)[CH2:3][CH2:2]2.[N:13]12CCC(CO)(CC1)CC2.S([O-])(=O)(=O)C.[C-]#N.[Na+]>CN(C)C=O>[N:1]12[CH2:8][CH2:7][C:4]([CH2:9][C:10]#[N:13])([CH2:5][CH2:6]1)[CH2:3][CH2:2]2
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8929Sodium CyanideHCID 85257MethanesulfonateHCID 1413111-Azabicyclo(2.2.2)octane-4-methanolHCID 220566712-(Quinuclidin-4-yl)acetyl chloride

생성물 1

HCID 220566352-{1-Azabicyclo[2.2.2]octan-4-yl}acetonitrile

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

2-(Quinuclidin-4-yl)acetyl chloride may be made by converting (quinuclidin-4-yl)methanol (vide supra) to the mesylate (methanesulfonylchloride/triethylamine in chloroform) which is then treated with sodium cyanide in dimethylformamide to form (quinuclidin-4-yl)acetonitrile. Heating this in ethanol saturated with hydrogen chloride gas produces the corresponding ethyl ester which is hydrolyzed to the acid by treatment with 6N hydrochloric acid. Finally, the acid is converted to the acid chloride as described above.

출처 및 근거

ORD 기록
ord-34d811726af34d329b91396f5db0e73a
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08114891B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차출처 및 근거반응 노트