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alpha-Bromo-2-nitrotoluene → Ethyl (2-nitrobenzyl)aminoacetate

HRID 2417452
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인쇄 미리보기

반응식

HRID 2417452 반응식
Cl.[CH2:2]([O:4][C:5](=[O:8])[CH2:6][NH2:7])[CH3:3].[N+:9]([C:12]1[CH:19]=[CH:18][CH:17]=[CH:16][C:13]=1[CH2:14]Br)([O-:11])=[O:10].C(=O)([O-])O.[Na+]>C(O)C>[N+:9]([C:12]1[CH:19]=[CH:18][CH:17]=[CH:16][C:13]=1[CH2:14][NH:7][CH2:6][C:5]([O:4][CH2:2][CH3:3])=[O:8])([O-:11])=[O:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 77569alpha-Bromo-2-nitrotolueneHCID 516892Sodium BicarbonateHCID 2723640Glycine ethyl ester, hydrochloride

생성물 1

HCID 13236074Ethyl (2-nitrobenzyl)aminoacetate

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
70 °C

실험 절차

6.35 g (45.4 mmol) of glycine ethyl ester hydrochloride, 2.45 g (11.3 mmol) of 2-nitrobenzyl bromide and 4.75 g (56.5 mmol) of sodium hydrogencarbonate were dissolved in ethanol, and the obtained solution was stirred at 70° C. overnight. The reaction solution was filtered, and the obtained filtrate was treated with ethyl acetate as the extracting solvent by an ordinary method to obtain the crude product. After the purification by the silica gel column chromatography, the title compound was obtained.

후처리

  1. filtrationThe reaction solution was filtered
  2. additionthe obtained filtrate was treated with ethyl acetate as the extracting solvent by an ordinary method
  3. customto obtain the crude product
  4. customAfter the purification by the silica gel column chromatography

출처 및 근거

ORD 기록
ord-09d7d5fc5903440caa890190c49bcd03
출처 데이터셋
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06825191B2

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