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1-tert-Butyl-2-(2-nitrophenoxy)benzene → HCID 5104180, 화합물

HRID 2377809
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인쇄 미리보기

반응식

HRID 2377809 반응식
[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[O:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[N+:18]([O-])=O)([CH3:4])([CH3:3])[CH3:2]>CO.C1COCC1.[Pd]>[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[O:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[NH2:18])([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 154152661-tert-Butyl-2-(2-nitrophenoxy)benzene

생성물 1

HCID 5104180HCID 5104180, 화합물수율 61.8%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 21899815MeOH tetrahydrofuran용매

실험 절차

To a solution of 1-tert-butyl-2-(2-nitrophenoxy)benzene (˜20 g, crude) in MeOH/THF (1:1, 200 mL) was added 10% Pd/C (2 g). The mixture was hydrogenated under 75 psi overnight. The mixture was filtered through Celite® cake and the filtrate was evaporated to give the crude product as a black oil. Purification by flash chromatography (0-30% EtOAc/hexane) provided 135a (11 g) as a brown solid.

후처리

  1. customwas hydrogenated under 75 psi overnight
  2. filtrationThe mixture was filtered through Celite® cake
  3. customthe filtrate was evaporated
  4. customto give the crude product as a black oil
  5. customPurification by flash chromatography (0-30% EtOAc/hexane)

출처 및 근거

ORD 기록
ord-4cd880e7e7154078892d2a2b9658f812
출처 데이터셋
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07470712B2

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