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2-Nitro-4-(thiophen-2-yl)aniline → 4-(Thiophen-2-yl)benzene-1,2-diamine

HRID 509184
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인쇄 미리보기

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HRID 509184 반응식
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[CH:12]=[CH:11][C:9]([NH2:10])=[C:8]([N+:13]([O-])=O)[CH:7]=1.[H][H]>[Pd]>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]1[CH:7]=[C:8]([NH2:13])[C:9]([NH2:10])=[CH:11][CH:12]=1
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참가 물질

4

반응물 2

HCID 226648312-Nitro-4-(thiophen-2-yl)anilineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 130078054-(Thiophen-2-yl)benzene-1,2-diamine수율 90%

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

To a solution of 4-thienyl-2-nitroaniline (1 equiv, 400 mg, 1.82 mmol) was added 10% Pd/C (0.05 equiv, 97 mg, 0.09 mmol). The resulting suspension was stirred for overnight over 1 atm of hydrogen. The solids were filtered through celite pad and the filtrate was concentrated under vacuum. The crude material was purified by silica gel column chromatography with gradient of MeOH (0-10%) in CH2Cl2 to afford compound 30 (310 mg, 90%) and a white solid. LRMS (ESI): (calc) 190.2 (found) 191.0 (MH)+.

후처리

  1. filtrationThe solids were filtered through celite pad
  2. concentrationthe filtrate was concentrated under vacuum
  3. customThe crude material was purified by silica gel column chromatography with gradient of MeOH (0-10%) in CH2Cl2

출처 및 근거

ORD 기록
ord-037a3ffdd9f646d0a19cd473696eb089
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09096565B2

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