Formaldehyde → 1-Nitro-2-phenylethane

HRID 1367633

反応式

HRID 1367633 の反応式
C(O)(=O)C.C(O)(=O)C.C(NCCNCC1C=CC=CC=1)C1C=CC=CC=1.[N+:27]([CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37]CCCCCCCCCC)([O-:29])=[O:28].C=O>C1(C)C=CC=CC=1.CO>[N+:27]([CH2:30][CH2:31][C:32]1[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=1)([O-:29])=[O:28]

参加物

5

反応物 3

HCID 712Formaldehyde2 回HCID 312281,2-Ethanediamine, N1,N2-bis(phenylmethyl)-, acetate (1:2)HCID 115439441-Nitrooctadecane

生成物 1

HCID 802081-Nitro-2-phenylethane収率 222.9%

試薬・触媒・溶媒 1

HCID 21867641Toluene methanol溶媒

実験手順

In a 500 mL round-bottom flask N,N′-dibenzylethylenediamine diacetate (4.78 g, 13 mmol) and 1-nitrooctadecane (3, 3.97 g, 13 mmol) are dissolved in 1:1 toluene/methanol (100 mL). Paraformaldehyde (1.39 g, 46.5 mmol) is added portionwise to the solution and the resulting suspension is refluxed. The mixture becomes homogeneous (dissolution of paraformaldehyde) and after 3 h at reflux, the mixture is cooled and evaporated in vacuo. The residue is recrystallized from ethanol, obtaining pure 4 (4.38 g, 61%) as colourless solid. M.p. 70-72° C. (EtOH), ESI-MS: 586 (MNa+), 564 (MH+); (Calc. for C36H57N3O2: 563 u.m.a.).

後処理

  1. temperaturethe resulting suspension is refluxed
  2. temperatureafter 3 h at reflux
  3. temperaturethe mixture is cooled
  4. customevaporated in vacuo
  5. customThe residue is recrystallized from ethanol

出典と根拠

ORDレコード
ord-5f656734956b48079d7aad7f360395be
出典データセット
uspto-grants-2011_02
特許番号
US07893223B2

関連ノート

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