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

O-ethylhydroxylamine hydrochloride → (1-azabicyclo-[2,2,2]-octan-3-yl)-ethanone O-ethyloxime hydrochloride

HRID 2081242
노트
인쇄 미리보기

반응식

HRID 2081242 반응식
[ClH:1].[C:2]([CH:5]1[CH:10]2[CH2:11][CH2:12][N:7]([CH2:8][CH2:9]2)[CH2:6]1)(=O)[CH3:3].Cl.[CH2:14]([O:16][NH2:17])[CH3:15]>CO>[ClH:1].[CH2:14]([O:16][N:17]=[C:2]([CH:5]1[CH:10]2[CH2:11][CH2:12][N:7]([CH2:8][CH2:9]2)[CH2:6]1)[CH3:3])[CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 76850O-ethylhydroxylamine hydrochlorideHCID 197994593-Acetyl quinuclidine hydrochloride

생성물 1

HCID 86744768(1-azabicyclo-[2,2,2]-octan-3-yl)-ethanone O-ethyloxime hydrochloride

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

1.9 g of 3-acetyl quinuclidine hydrochloride and 0.98 g of O-ethylhydroxylamine hydrochloride are heated for 20 minutes to reflux in 30 cm3 of methanol, followed by concentrating to dryness and purifying by chromatography on alumina (eluant: methylene chloride-methanol 9-1). The reaction medium is acidified using gaseous hydrochloric acid, then evaporated to dryness. After crystallizing from ethanol, filtering, and rinsing with ether, 1.3 g of expected product is recovered. M.p.=198°-200° C.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. concentrationby concentrating to dryness
  2. custompurifying by chromatography on alumina (eluant: methylene chloride-methanol 9-1)
  3. customevaporated to dryness
  4. customAfter crystallizing from ethanol
  5. filtrationfiltering
  6. washrinsing with ether, 1.3 g of expected product
  7. customis recovered

출처 및 근거

ORD 기록
ord-e2079ee0f6104709a5d0ce29c2d23382
출처 데이터셋
uspto-grants-1993_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05183893

반응 노트

불러오는 중…