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Triethylamine → N-ethoxalyl-N-isopropyl-2-nitroaniline

HRID 1073080
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HRID 1073080 반응식
[CH:1]([NH:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[N+:11]([O-:13])=[O:12])([CH3:3])[CH3:2].C(N(CC)CC)C.[C:21](Cl)([C:23]([O:25][CH2:26][CH3:27])=[O:24])=[O:22]>O1CCCC1>[C:21]([N:4]([CH:1]([CH3:3])[CH3:2])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[N+:11]([O-:13])=[O:12])([C:23]([O:25][CH2:26][CH3:27])=[O:24])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 20884Ethoxalyl chlorideHCID 10583518N-Isopropyl-2-nitroaniline

생성물 1

HCID 14853709N-ethoxalyl-N-isopropyl-2-nitroaniline

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred ice-cooled solution of 2-isopropylamino-nitrobenzene (19.5 g, 0.1 mole) and triethylamine (15 ml 0.11 mole) in tetrahydrofurane (THF, 200 ml) was dropwise added ethoxalyl chloride. The ice bath was removed and the mixture was heated to reflux for 3 hours. The precipitated triethylammonium chloride was filtered off and the filtrate was evaporated in vacuo to give the title compound as an oil.

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후처리

  1. customThe ice bath was removed
  2. temperaturethe mixture was heated
  3. temperatureto reflux for 3 hours
  4. filtrationThe precipitated triethylammonium chloride was filtered off
  5. customthe filtrate was evaporated in vacuo

출처 및 근거

ORD 기록
ord-dcd550a6b27c4a669a01a4a7880fe1e5
출처 데이터셋
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04968682

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