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1-溴辛烷 → N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamine

HRID 525980
笔记
打印预览

反应方程式

HRID 525980 反应方程式
[C:1]1([NH2:12])[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([NH2:11])[C:5]=2[CH:4]=[CH:3][CH:2]=1.Br[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21].C(=O)([O-])[O-].[K+].[K+]>C(O)CCC.[I-].[K+]>[CH2:14]([N:12]([CH2:9][CH2:10][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH3:6])[C:1]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([N:11]([CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])[C:5]=2[CH:4]=[CH:3][CH:2]=1)[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21]
参与物反应条件实验过程后处理来源与证据反应笔记

参与物

6

反应物 3

HCID 81401-溴辛烷HCID 11430碳酸钾HCID 167201,5-萘二胺

产物 1

HCID 68441382N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamine收率 38.3%

试剂、催化剂与溶剂 2

HCID 4875碘化钾催化剂HCID 263丁醇溶剂

反应条件

温度
110 °C

实验过程

Naphthalene-1,5-diamine (3.14 g, 19.8 mmol), 1-bromooctane (25.25 g, 0.130 mol), potassium carbonate (11.79 g, 85.3 mmol), and potassium iodide (0.05 g, 0.30 mmol) was stirred in dry butanol (150 ml) and heated to 110° C. for 36 h. The reaction was quenched with water and extracted with ether three times. The combined organic phase was washed three times with water and evaporated to give black oil which was distilled under reduced pressure at 90° C. to yield a black tar. This was purified with flash chromatography using hexane as mobile phase to obtain colourless oil which crystallised to yield N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamine (2.3 g, 3.79 mmol) as white crystals. 1H-NMR (CDCl3, δ): 0.85 (t, 12H), 1.0-1.4 (m, 40H), 1.4-1.6 (m, 8H), 3.08 (t, 8H), 7.1 (d, 2H), 7.35 (t, 2H), 8.01 (d, 2H) MS MALDI-TOF (m/z): 606.574

后处理

  1. customThe reaction was quenched with water
  2. extractionextracted with ether three times
  3. washThe combined organic phase was washed three times with water
  4. customevaporated
  5. customto give black oil which
  6. distillationwas distilled under reduced pressure at 90° C.
  7. customto yield a black tar
  8. customThis was purified with flash chromatography
  9. customto obtain colourless oil which
  10. customcrystallised

来源与证据

ORD记录
ord-e20de384567c4138967ddc336962212b
来源数据集
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
专利号
US09343198B2

反应笔记

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本页导航参与物反应条件实验过程后处理来源与证据反应笔记