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

5-Nitro-4,7-dimethyl-1,3-benzodioxole → 5-Amino-4,7-dimethyl-1,3-benzodioxole

HRID 1376555
노트
인쇄 미리보기

반응식

HRID 1376555 반응식
[N+:1]([C:4]1[CH:12]=[C:11]([CH3:13])[C:7]2[O:8][CH2:9][O:10][C:6]=2[C:5]=1[CH3:14])([O-])=O.[H][H]>[Pd].C(O)C>[NH2:1][C:4]1[CH:12]=[C:11]([CH3:13])[C:7]2[O:8][CH2:9][O:10][C:6]=2[C:5]=1[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 218404755-Nitro-4,7-dimethyl-1,3-benzodioxoleHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 150610985-Amino-4,7-dimethyl-1,3-benzodioxole수율 99.9%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A mixture of 1.88 g of 5-nitro-4,7-dimethyl-1,3-benzodioxole and 0.19 g of 10% palladium on carbon in 200 mL of ethanol is placed under a 50 psi hydrogen atmosphere. The mixture is shaken for 90 minutes at room temperature. The reaction mixture is filtered through Celite to yield a brownish solution. Concentration under reduced pressure affords 1.59 g of 5-amino-4,7-dimethyl-1,3-benzodioxole.

후처리

  1. filtrationThe reaction mixture is filtered through Celite
  2. customto yield a brownish solution
  3. concentrationConcentration under reduced pressure

출처 및 근거

ORD 기록
ord-bc99ec18769f4c8e9a650dd71a101f80
출처 데이터셋
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05663189

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트