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2-Chloro-5-methoxy-4-nitrobenzoic acid → 4-Amino-2-chloro-5-methoxybenzoic acid

HRID 2234484
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HRID 2234484 반응식
[Cl:1][C:2]1[CH:10]=[C:9]([N+:11]([O-])=O)[C:8]([O:14][CH3:15])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]>CCO.[Pt]>[NH2:11][C:9]1[C:8]([O:14][CH3:15])=[CH:7][C:3]([C:4]([OH:6])=[O:5])=[C:2]([Cl:1])[CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 580563702-Chloro-5-methoxy-4-nitrobenzoic acid2회

생성물 1

HCID 670035054-Amino-2-chloro-5-methoxybenzoic acid

시약·촉매·용매 2

HCID 23939Platinum촉매HCID 702Ethanol용매

실험 절차

2-chloro-5-methoxy-4-nitro-benzoic acid (Intermediate 218; 762 mg, 3.8 mmol) was dissolved in EtOH (20 mL) and a catalytic amount of 5% Pt on carbon added under an inert atmosphere. The solution was de-gassed and stirred under an atmosphere of hydrogen at room temperature overnight. The catalyst was filtered off and washed with EtOH and solvent evaporated and the resultant material dried under vacuum to yield the title compound as an off-white solid. (617 mg, 98%)

후처리

  1. customThe solution was de-gassed
  2. filtrationThe catalyst was filtered off
  3. washwashed with EtOH and solvent
  4. customevaporated
  5. dry with materialthe resultant material dried under vacuum

출처 및 근거

ORD 기록
ord-bbe11f1fb4624526a73f895cef25d6b9
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07709471B2

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