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

Hydroxylamine → 1-[4-(4-Chloro-2-fluoro-phenoxy)-phenyl]-ethanone-oxime

HRID 1406332
노트
인쇄 미리보기

반응식

HRID 1406332 반응식
[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([C:13](=O)[CH3:14])=[CH:9][CH:8]=2)=[C:4]([F:18])[CH:3]=1.[NH2:19][OH:20]>C(O)C>[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([C:13](=[N:19][OH:20])[CH3:14])=[CH:9][CH:8]=2)=[C:4]([F:18])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 787HydroxylamineHCID 667903211-(4-(4-Chloro-2-fluorophenoxy)phenyl)ethanone

생성물 1

HCID 866588121-[4-(4-Chloro-2-fluoro-phenoxy)-phenyl]-ethanone-oxime

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 3.4 g (12.8 mmol) of 1-[4-(4-chloro-2-fluoro-phenoxy)-phenyl]-ethanone and 3.0 mL hydroxylamine solution (50% in water) in 100 mL ethanol was refluxed for five hours. Then the mixture was evaporated to dryness, the residue was combined with approx. 15 mL water and extracted three times with 10 mL ethyl acetate. The extracts were washed with saturated sodium chloride solution, dried and evaporated down. The product thus obtained was reacted further without any further purification.

후처리

  1. temperaturewas refluxed for five hours
  2. customThen the mixture was evaporated to dryness
  3. extractionextracted three times with 10 mL ethyl acetate
  4. washThe extracts were washed with saturated sodium chloride solution
  5. customdried
  6. customevaporated down
  7. customThe product thus obtained
  8. customwas reacted further without any further purification

출처 및 근거

ORD 기록
ord-e4b5dc36bc5c41c088d3f3b12c768717
출처 데이터셋
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08916589B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트