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

Ammonium formate → 1-N-(propan-2-yl)benzene-1,2-diamine

HRID 1521728
노트
인쇄 미리보기

반응식

HRID 1521728 반응식
[N+:1]([C:4]1[CH:13]=[CH:12][CH:11]=[CH:10][C:5]=1[NH:6][CH:7]([CH3:9])[CH3:8])([O-])=O.C([O-])=O.[NH4+]>C(O)C.[Pd]>[CH3:9][CH:7]([NH:6][C:5]1[C:4]([NH2:1])=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 2723923Ammonium formateHCID 10583518N-Isopropyl-2-nitroaniline

생성물 1

HCID 105587871-N-(propan-2-yl)benzene-1,2-diamine수율 80%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To a solution of 2-nitro-N-(propan-2-yl)aniline (828 mg, 4.6 mmol) in ethanol (10 mL) under a nitrogen atmosphere is carefully added 20% palladium on carbon (50 mg, Degussa type) followed by ammonium formate (1.4 g, 23 mmol) and the reaction is stirred for 16 h. The suspension is carefully filtered through a bed of Celite and the filter cake is rinsed with additional ethanol (10 mL). The filtrate is concentrated and the residue is partitioned between H2O and ethyl acetate. The organic layer is dried (Na2SO4) and concentrated and the residue is purified by chromatography through a short bed of silica gel using 5% methanol/CH2Cl2 affords the title compound (552 mg, 80%) as an oil.

후처리

  1. filtrationThe suspension is carefully filtered through a bed of Celite
  2. washthe filter cake is rinsed with additional ethanol (10 mL)
  3. concentrationThe filtrate is concentrated
  4. customthe residue is partitioned between H2O and ethyl acetate
  5. dry with materialThe organic layer is dried (Na2SO4)
  6. concentrationconcentrated
  7. customthe residue is purified by chromatography through a short bed of silica gel using 5% methanol/CH2Cl2

출처 및 근거

ORD 기록
ord-b0a9c5ed10184b5ba39c7cb47364b683
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09073926B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트