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Diethylamine → HCID 74217918、化合物

HRID 1514030
ノート
印刷プレビュー

反応式

HRID 1514030 の反応式
[CH2:1]([NH:3][CH2:4][CH3:5])[CH3:2].[OH-].[Na+].[CH2:8]([O:14][C:15](Cl)=[O:16])[CH2:9][CH:10]=[CH:11][CH2:12][CH3:13]>C(OCC)C>[CH2:8]([O:14][C:15](=[O:16])[N:3]([CH2:4][CH3:5])[CH2:1][CH3:2])[CH2:9][CH:10]=[CH:11][CH2:12][CH3:13]
参加物反応条件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 8021DiethylamineHCID 14798Sodium HydroxideHCID 54291304Chloroformic acid hex-3-enyl ester

生成物 1

HCID 74217918HCID 74217918、化合物収率 92%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

反応条件

温度
0 °C

実験手順

Diethylamine (9.1 g, 125 mmol, 1.25 equiv.) was added to a 2%-aqueous NaOH-solution (200 ml) and the resulting mixture was cooled to 0° C. (icebath). At this temperature chloroformic acid hex-3-enyl ester (16.2 g, 100 mmol) in diethyl ether (200 ml) was added over a period of 35 min. After complete addition, the cooling bath was removed and stirring was continued for 1.5 h. The mixture was acidified with 2N aqueous HCl-solution, the phases separated and the organic phase was washed with brine and dried over MgSO4. The crude product was purified via fractionated distillation (74-76° C./0.05 mbar) to yield 18.2 g (92%) of product.

後処理

  1. additionAfter complete addition
  2. customthe cooling bath was removed
  3. customthe phases separated
  4. washthe organic phase was washed with brine
  5. dry with materialdried over MgSO4
  6. distillationThe crude product was purified via fractionated distillation (74-76° C./0.05 mbar)

出典と根拠

ORDレコード
ord-3e3457c745664905b65a2842fc51d625
出典データセット
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08222200B2

反応ノート

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