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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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N,N-Dimethyl-3-nitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline → N1,N1-dimethyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1,3-diamine

HRID 1052618
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인쇄 미리보기

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HRID 1052618 반응식
[CH3:1][N:2]([CH3:21])[C:3]1[CH:8]=[C:7]([B:9]2[O:13][C:12]([CH3:15])([CH3:14])[C:11]([CH3:17])([CH3:16])[O:10]2)[CH:6]=[C:5]([N+:18]([O-])=O)[CH:4]=1>C(OCC)(=O)C.[Pd]>[CH3:21][N:2]([CH3:1])[C:3]1[CH:8]=[C:7]([B:9]2[O:10][C:11]([CH3:16])([CH3:17])[C:12]([CH3:15])([CH3:14])[O:13]2)[CH:6]=[C:5]([NH2:18])[CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 90102809N,N-Dimethyl-3-nitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline

생성물 1

HCID 131074365N1,N1-dimethyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzene-1,3-diamine수율 101.3%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

N,N-Dimethyl-3-nitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (356 mg, 1.22 mmol) was dissolved in 50 ml of ethyl acetate. This mixture was hydrogenated in an H-Cube® apparatus using 10% palladium on carbon as catalyst at 2-3 bar. The solvent was evaporated to give 324 mg (99% yield) of the title compound as a white solid. Purity 100%.

후처리

  1. customThe solvent was evaporated

출처 및 근거

ORD 기록
ord-da1c63d64a8e4410bf752346735afa6b
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09388189B2

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