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Ethylamine → N-ethyl-2-methyl-2-(4-nitrophenyl)propan-1-amine

HRID 2423225
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HRID 2423225 반응식
[CH3:1][C:2]([C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[CH:8][CH:7]=1)([CH3:5])[CH:3]=O.[CH2:15]([NH2:17])[CH3:16].[BH4-].[Na+]>CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-].C(O)C>[CH2:15]([NH:17][CH2:3][C:2]([CH3:5])([C:6]1[CH:11]=[CH:10][C:9]([N+:12]([O-:14])=[O:13])=[CH:8][CH:7]=1)[CH3:1])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6341EthylamineHCID 4311764Sodium borohydrideHCID 15074483HCID 15074483, 화합물

생성물 1

HCID 67243335N-ethyl-2-methyl-2-(4-nitrophenyl)propan-1-amine수율 98%

시약·촉매·용매 2

HCID 11026Titanium isopropoxide촉매HCID 702Ethanol
용매

실험 절차

In a 250 mL round bottom flask was charged 2-methyl-2-(4-nitrophenyl)propanal (2.00 g, 10.4 mmol), absolute ethanol (30 mL), ethyl amine solution (20.7 mL, 1M in THF). Titanium isopropoxide (6.2 mL, 20.7 mmol) was added and the mixture was stirred at ambient temperature for 1 h. Sodium borohydride (1.17 g, 31 mmol) was added and the reaction stirred for an additional 1 h. The reaction was quenched by pouring into 10% ammonium hydroxide solution (25 mL), ethyl acetate was added and the solids were removed by filtration, the pad was washed once with ethyl acetate and the solvent was concentrated in vacuo to give N-ethyl-2-methyl-2-(4-nitrophenyl)propan-1-amine (2.25 g, 98%). LC/MS (ESI+) 223 (M+H)+.

후처리

  1. stirringthe reaction stirred for an additional 1 h
  2. customThe reaction was quenched
  3. additionby pouring into 10% ammonium hydroxide solution (25 mL), ethyl acetate
  4. additionwas added
  5. customthe solids were removed by filtration
  6. washthe pad was washed once with ethyl acetate
  7. concentrationthe solvent was concentrated in vacuo

출처 및 근거

ORD 기록
ord-398234dfd7dd4d3a9b4c31a809b6e441
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07960569B2

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