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Hexane → 4-[(2-Methoxyethoxy)methoxy]aniline

HRID 1603241
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반응식

HRID 1603241 반응식
[CH3:1][O:2][CH2:3][CH2:4][O:5][CH2:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([N+:14]([O-])=O)=[CH:10][CH:9]=1.C([O-])=O.[NH4+].CCCCCC>C(O)C.[Pd]>[CH3:1][O:2][CH2:3][CH2:4][O:5][CH2:6][O:7][C:8]1[CH:9]=[CH:10][C:11]([NH2:14])=[CH:12][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 8058HexaneHCID 2723923Ammonium formateHCID 196090861-[(2-methoxyethoxy)methoxy]-4-nitroBenzene

생성물 1

HCID 131356894-[(2-Methoxyethoxy)methoxy]aniline수율 75%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매2회
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실험 절차

A mixture of 200 mg (0.88 mmol) of 1-[(2-methoxyethoxy) methoxy]-4-nitrobenzene (21), 100 mg of 10% Pd/C and 550 mg (8.7 mmol) of ammonium formate in 10 mL of absolute ethanol was stirred at room temperature for 18 hours. The reaction mixture was diluted with 100 mL of absolute ethanol and passed through a small pad of celite. The filtrate was concentrated and purified by silica gel column chromatography using 8:2 ethyl acetate:hexane as the eluent to yield 130 mg (0.65 mmol, 75%) of 4-[(2-methoxyethoxy)methoxy]benzenamine (22). NMR, IR and MS data confirmed compound identity.

후처리

  1. concentrationThe filtrate was concentrated
  2. custompurified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-b72cad446df04ae38b4f6c628012200f
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05986094

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