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Water → 1-Nitrotridecane

HRID 264115
ノート
印刷プレビュー

反応式

HRID 264115 の反応式
[N:1]([O-:3])=[O:2].[Na+].Br[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].O>CN(C)C=O>[N+:1]([CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH3:6])([O-:3])=[O:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 130001-BromotridecaneHCID 23668193Sodium Nitrite

生成物 1

HCID 108233151-Nitrotridecane

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a stirred, room temperature suspension of sodium nitrite (227 g, 3.29 mol) in dimethylformamide (3.8 L) was added 1-bromotridecane (514.51 g, 1.95435 mol), and the mixture was stirred for 6 hours. The mixture was poured into cold water (8 L) and extracted with petroleum ether (2×2 L). The organic layer was washed with water (2 L), saturated sodium chloride, dried (MgSO4), and rotoevaporated to a yellow oil. The oil was distilled in vacuo to give another oil; yield 171.9 g, bp 101°-120° C. (0.2 mm Hg). The oil was chromatographed on silica gel (3.0 kg, 230-400 mesh) using ether/ethyl acetate (100:1, 4×2 L; 80:1, 4×2 L; 50:1, 7×2 L) to give a clear colorless oil; yield 109.8 g (24.5%).

後処理

  1. extractionextracted with petroleum ether (2×2 L)
  2. washThe organic layer was washed with water (2 L), saturated sodium chloride
  3. dry with materialdried (MgSO4)
  4. distillationThe oil was distilled in vacuo
  5. customto give another oil
  6. customThe oil was chromatographed on silica gel (3.0 kg, 230-400 mesh)
  7. customto give a clear colorless oil

出典と根拠

ORDレコード
ord-37458cf00f524c68b0fbb36c56869bf5
出典データセット
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05646170

反応ノート

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