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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Diethyl Ether → [(2,4-Dimethoxyphenyl)methyl](methyl)amine

HRID 1644631
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HRID 1644631 반응식
[CH3:1][O:2][C:3]1[CH:12]=[C:11]([O:13][CH3:14])[CH:10]=[CH:9][C:4]=1[CH2:5][NH:6][CH:7]=O.[AlH4-].[Li+].CCOCC>>[CH3:1][O:2][C:3]1[CH:12]=[C:11]([O:13][CH3:14])[CH:10]=[CH:9][C:4]=1[CH2:5][NH:6][CH3:7]
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참가 물질

4

반응물 3

HCID 3283Diethyl EtherHCID 28112Lithium aluminum hydrideHCID 21465904N-(2,4-Dimethoxy-benzyl)-formamide

생성물 1

HCID 2416536[(2,4-Dimethoxyphenyl)methyl](methyl)amine수율 82%

실험 절차

N-(2,4-Dimethoxy-benzyl)-formamide (0.50 g, 2.6 mmol) was added slowly to a suspension of the lithium tetrahydroaluminate (0.19 g, 5.1 mmol) in ether (30 mL, 200 mmol) at −78° C. The reaction mixture was warmed slowly to rt and stirred at rt under an atmosphere of Argon over night. The reaction was quenched at 0° C. by the sequential addition of 0.19 ml of H2O, 0.19 ml of 15% aq NaOH solution, and 0.57 ml of the H2O. The inorganic solids were removed by filtration and washed with ether. The ether filtrate was washed with water and brine, dried over Na2SO4. Evaporation of the solvent gave the product as a pale yellow oil (0.38 g, 82%).

후처리

  1. customThe reaction was quenched at 0° C. by the sequential addition of 0.19 ml of H2O, 0.19 ml of 15% aq NaOH solution, and 0.57 ml of the H2O
  2. customThe inorganic solids were removed by filtration
  3. washwashed with ether
  4. washThe ether filtrate was washed with water and brine
  5. dry with materialdried over Na2SO4
  6. customEvaporation of the solvent

출처 및 근거

ORD 기록
ord-cce8caa23ce247cdbcff8a4bea972154
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08124610B2

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