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Carbon Dioxide → HCID 21475509、化合物

HRID 440619
ノート
印刷プレビュー

反応式

HRID 440619 の反応式
C(Cl)(=O)C([Cl:4])=O.[ClH:7].[CH3:8][N:9]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16](O)=[O:17])[CH3:10].Cl.C(=O)=O>>[ClH:4].[CH3:8][N:9]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]([Cl:7])=[O:17])[CH3:10]
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 4

HCID 280Carbon DioxideHCID 313Hydrochloric AcidHCID 65578Oxalyl chlorideHCID 199777516-(Dimethylamino)hexanoic acid hydrochloride

生成物 1

HCID 21475509HCID 21475509、化合物

反応条件

温度
30 °C

実験手順

Oxalyl chloride (3367.33 g, 26.53 mol) is placed in a 5000 mL three-necked round-bottomed flask equipped with a reflux condenser, internal thermometer, mechanical stirrer, and argon inlet. 6-(N,N-Dimethylamino)hexanoic acidhydrochloride (1146.00 g, 5.86 mol) is added over 3 h while maintaining the reaction temperature between 25-35 ° C. As reaction takes place, HCl, CO2, and CO are swept away from the mixture with argon. After addition is complete, the mixture is cooled to room temperature over 45 min. Excess oxalyl chloride is removed first by rotary evaporation at 50° C. (water aspirator vacuum) and then by Kugelrohr distillation at 60° C. (0.3 mm Hg) for 3 h. A quantitative yield of 3 is isolated as a dark red oil that solidifies on standing.

後処理

  1. customequipped with a reflux condenser
  2. customAs reaction
  3. additionAfter addition
  4. temperaturethe mixture is cooled to room temperature over 45 min
  5. customExcess oxalyl chloride is removed first by rotary evaporation at 50° C. (water aspirator vacuum)
  6. distillationby Kugelrohr distillation at 60° C. (0.3 mm Hg) for 3 h

出典と根拠

ORDレコード
ord-1e1d38c615d940ce82dc5f522df2c864
出典データセット
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05520835

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート