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Nitric Acid → 3-Nitroxypropylamine nitrate

HRID 1362797
ノート
印刷プレビュー

反応式

HRID 1362797 の反応式
[NH2:1][CH2:2][CH2:3][CH2:4][OH:5].[N+:6]([O-:9])([OH:8])=[O:7]>C(OC(=O)C)(=O)C>[N+:6]([O-:9])([OH:8])=[O:7].[N+:6]([O:5][CH2:4][CH2:3][CH2:2][NH2:1])([O-:8])=[O:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 944Nitric AcidHCID 90863-Amino-1-propanol

生成物 1

HCID 220145913-Nitroxypropylamine nitrate収率 80%

試薬・触媒・溶媒 1

HCID 7918Acetic Anhydride溶媒

実験手順

A solution of 3-amino-1-propanol (6.17 g, 82.2 mmol) was added, drop-wise, to an ice-cooled solution of fuming nitric acid (90%, 12 mL) in acetic anhydride (50 mL). The reaction was stirred in an ice-bath for 10 minutes and then at room temperature for 10 minutes. The solvent was evaporated under vacuum at 40° C. The residue was stirred in diethylether (200 mL) until the product precipitated. The mixture was filtered and the white crystalline solid was dried in vacuo to give the title compound (12.1 g, 80% yield). 1H NMR (300 MHz, DMSO-d6) δ 4.57 (br. t, 2H), 2.8-3.0 (m, 2H), 1.98-1.93 (m, 2H). 13C NMR (75 MHz, DMSO-d6) δ 70.9, 36.1, 24.5. MS m/z 121 (M−NO3)+.

後処理

  1. waitat room temperature for 10 minutes
  2. customThe solvent was evaporated under vacuum at 40° C
  3. stirringThe residue was stirred in diethylether (200 mL) until the product
  4. customprecipitated
  5. filtrationThe mixture was filtered
  6. customthe white crystalline solid was dried in vacuo

出典と根拠

ORDレコード
ord-237f7a1b7c7b42ef84c6be7b397488e5
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07883714B2

反応ノート

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