Ethanolamine → 2-Octyl-2-oxazoline

HRID 355460

反応式

HRID 355460 の反応式
[CH2:1]([C:9]#[N:10])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[OH:11][CH2:12][CH2:13]N>C([O-])(=O)C.[Zn+2].C([O-])(=O)C.C(O)CCC>[CH2:1]([C:9]1[O:11][CH2:12][CH2:13][N:10]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]

参加物

5

反応物 2

HCID 700EthanolamineHCID 16715Nonanenitrile

生成物 1

HCID 229995422-Octyl-2-oxazoline収率 47%

試薬・触媒・溶媒 2

HCID 11192Zinc Acetate触媒HCID 2631-Butanol溶媒

反応条件

温度
120 °C

実験手順

A mixture of octyl cyanide (75.0 g, 0.539 mol), anhydrous zinc acetate (2.47 g, 0.0134 mol) and 1-butanol (270 ml) was stirred at 120° C. under nitrogen. To this mixture was dropwisely added 2-hydroxyethyl amine (39.5 g, 0.647 mol) in 20 min., and the resulting mixture was stirred at 120° C. for 40 h. The resulting admixture was distilled under reduced pressure three times. The fraction at 75°-80° C./0.2 mmHg was collected to give 2-octyl-2-oxazoline as a colorless liquid (46 g, 47% yield). The product was again distilled under reduced pressure from calcium hydride: 1H NMR (CDCl3) delta 0.88 (5, J=6.6 Hz, 3H, CH3), 1.29 (m, 10H, CH2×8), 1.63 (t of t, J=6.6 and 6.9 Hz, 2H, CH2), 2.26 (t, J=7.2 Hz, 2H, CH2), 3.82 (t, J=9.6 Hz, 2H, CH2O), and 4.22 (t, J=9.6, 2H, CH2N).

後処理

  1. customin 20 min.
  2. stirringthe resulting mixture was stirred at 120° C. for 40 h
  3. distillationThe resulting admixture was distilled under reduced pressure three times
  4. customThe fraction at 75°-80° C./0.2 mmHg was collected

出典と根拠

ORDレコード
ord-d51ca538674445ba97caad9841933dbe
出典データセット
uspto-grants-1998_11
特許番号
US05830948

関連ノート

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