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

5-Fluoroindanone oxime → 5-Fluoro-2,3-dihydro-1H-inden-1-amine

HRID 375600
노트
인쇄 미리보기

반응식

HRID 375600 반응식
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[N:11]O)[CH2:6][CH2:5]2>C(O)(=O)C.[Zn]>[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[CH:7]([NH2:11])[CH2:6][CH2:5]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 736055205-Fluoroindanone oxime

생성물 1

HCID 166663285-Fluoro-2,3-dihydro-1H-inden-1-amine수율 96.3%

시약·촉매·용매 2

HCID 23994Zinc촉매HCID 176Acetic Acid용매

실험 절차

Zinc powder (20.2 g) was added during three hours to the stirred solution of the above oxime (20.2 g) in acetic acid (200 ml) which maintains the temperature at 25°-35° C. The resulting mixture was stirred an additional 12 hours at room temperature. The solids were removed by filtration and the filtrate concentrated in vacuo. The concentrated filtrate was partitioned between water and toluene and the aqueous phase adjusted to pH 12 with ammonium hydroxide and extracted with toluene. Solvent removal in vacuo gave 5-fluoro-1-aminoindan (17.8 g) as a colored oil.

후처리

  1. customat 25°-35° C
  2. customThe solids were removed by filtration
  3. concentrationthe filtrate concentrated in vacuo
  4. customThe concentrated filtrate was partitioned between water and toluene
  5. extractionextracted with toluene
  6. customSolvent removal in vacuo

출처 및 근거

ORD 기록
ord-308f788b92cc49588ca4ad24af84b0b0
출처 데이터셋
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05486541

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트