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Ethanolamine → 2-(Nitrooxy)ethylammonium nitrate

HRID 1362805
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HRID 1362805 반응식
[OH:1][CH2:2][CH2:3][NH2:4].[N+:5]([O-:8])([OH:7])=[O:6].CC(OC(C)=O)=O>CCOC(C)=O>[N+:5]([O-:8])([O-:7])=[O:6].[N+:5]([O:1][CH2:2][CH2:3][NH3+:4])([O-:7])=[O:6]
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참가 물질

5

반응물 3

HCID 700EthanolamineHCID 944Nitric AcidHCID 7918Acetic Anhydride

생성물 1

HCID 210759462-(Nitrooxy)ethylammonium nitrate

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
0 °C

실험 절차

2-Hydroxyethylamine (5 g, 81.9 mmol) in EtOAc (40 mL) was added drop-wise to a mixture of fuming HNO3 (18 g, 12 mL, 0.29 mol) and Ac2O (54 g, 50 mL, 0.53 mol) at −10° C. The reaction mixture was stirred at 0° C. for 10 minutes and at room temperature for 10 minutes. The solvent was evaporated in high vacuo at 40° C. The residue was sonicated with ether. The solid was filtered and washed with hexane to give the title compound as a white solid. Mp 92-94° C. 1H NMR (300 MHz, d6-DMSO) δ 7.71-8.25 (bs, 3H), 4.72 (t, J=5.0 Hz, 2H), 3.23 (d, J=5.0 Hz, 2H). 13C NMR (75 MHz, d6-DMSO) δ 70.9, 37.4.

후처리

  1. customThe solvent was evaporated in high vacuo at 40° C
  2. customThe residue was sonicated with ether
  3. filtrationThe solid was filtered
  4. washwashed with hexane

출처 및 근거

ORD 기록
ord-400c5bb3d38f4f12bee2141f8da67732
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07883714B2

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