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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methyl 3-nitronaphthalene-1-carboxylate → Methyl 3-aminonaphthalene-1-carboxylate

HRID 1010616
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HRID 1010616 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([C:14]([O:16][CH3:17])=[O:15])[C:7]2[C:12]([CH:13]=1)=[CH:11][CH:10]=[CH:9][CH:8]=2)([O-])=O>[Pd].C(O)C.ClCCl>[NH2:1][C:4]1[CH:5]=[C:6]([C:14]([O:16][CH3:17])=[O:15])[C:7]2[C:12]([CH:13]=1)=[CH:11][CH:10]=[CH:9][CH:8]=2
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참가 물질

5

반응물 1

HCID 260948Methyl 3-nitronaphthalene-1-carboxylate

생성물 1

HCID 23423661Methyl 3-aminonaphthalene-1-carboxylate

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 702Ethanol용매HCID 6344Dichloromethane용매

실험 절차

To 1.15 g (1.08 mmol) of 10% palladium on carbon was added a suspension of 11.6 g (50.0 mmol) of the above methyl 3-nitro-1-naphthoate in 150 mL of anhydrous ethanol and 40 mL of anhydrous dichloromethane. The resulting suspension was agitated under an atmosphere of hydrogen at 40 psi for 3 h during which time all solids dissolved. The reaction mixture was filtered through a plug of Celite®, which was subsequently washed with dichloromethane (300 mL). The combined filtrates were concentrated in vacuo to yield the title compound as a pale green gum which was used without further purification. LC/MS 202.1 (M+1).

후처리

  1. dissolutiondissolved
  2. filtrationThe reaction mixture was filtered through a plug of Celite®, which
  3. washwas subsequently washed with dichloromethane (300 mL)
  4. concentrationThe combined filtrates were concentrated in vacuo

출처 및 근거

ORD 기록
ord-a6ef63a589a340cd8bc6daaf0a29d7bc
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07977339B2

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