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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N-Ethyl-3-nitro PABA → 3-Amino-4-(ethylamino)benzoic acid

HRID 1591969
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HRID 1591969 반응식
[CH2:1]([NH:3][C:4]1[CH:12]=[CH:11][C:7]([C:8]([OH:10])=[O:9])=[CH:6][C:5]=1[N+:13]([O-])=O)[CH3:2]>C1COCC1.O.[Ni]>[NH2:13][C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][C:4]=1[NH:3][CH2:1][CH3:2])[C:8]([OH:10])=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 3729086N-Ethyl-3-nitro PABA

생성물 1

HCID 8544283-Amino-4-(ethylamino)benzoic acid

시약·촉매·용매 2

HCID 935Nickel촉매HCID 21881883Oxolane--water (1/1)용매

실험 절차

A solution of 1.56 g (7.4 mmol) of the title A compound 4-ethylamino-3-nitro-benzoic acid in 60 mL of THF/water (2:1) is hydrogenated at 20 psi over 300 mg of Raney nickel for 18 h. The catalyst is removed by filtration through Celite and the solvent is removed under reduced pressure to give 3-amino-4-ethylamino-benzoic acid as a dark solid. This material is used as such in the next step.

후처리

  1. customThe catalyst is removed by filtration through Celite
  2. customthe solvent is removed under reduced pressure

출처 및 근거

ORD 기록
ord-6d237297cbed410e884e3be43b602fb6
출처 데이터셋
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07291635B2

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