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

Perchloric Acid → 1-(2,2,2-Trifluoro-ethyl)-1,3-dihydro-indol-2-one

HRID 610077
노트
인쇄 미리보기

반응식

HRID 610077 반응식
[F:1][C:2]([F:16])([F:15])[CH2:3][N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6](=O)[C:5]1=[O:14].Cl(O)(=O)(=O)=O>[Pd].C(O)(=O)C>[F:16][C:2]([F:1])([F:15])[CH2:3][N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6][C:5]1=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24247Perchloric AcidHCID 19600971HCID 19600971, 화합물

생성물 1

HCID 196009761-(2,2,2-Trifluoro-ethyl)-1,3-dihydro-indol-2-one

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 176Acetic Acid용매

실험 절차

A mixture of 1-(2,2,2-trifluoro-ethyl)-1H-indole-2,3-dione (9.2 g, 40 mmol) and 10% palladium on carbon (2.4 g) in acetic acid (100 mL) and 70% perchloric acid (6.4 mL, 80 mmol) was hydrogenated in a Parr apparatus for 22 hours. The mixture was filtered through diatomaceous earth, diluted with water (1.5 L) and the precipitate was collected and dried. mp 155-162° C. Yield 7.5 g (87%).

후처리

  1. filtrationThe mixture was filtered through diatomaceous earth
  2. additiondiluted with water (1.5 L)
  3. customthe precipitate was collected
  4. customdried

출처 및 근거

ORD 기록
ord-71726128dbff49b89aca16c8a8f66f7a
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05998463

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트