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Carbon Dioxide → HCID 21475509, 화합물

HRID 864107
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HRID 864107 반응식
[C:1](Cl)(=O)[C:2]([Cl:4])=[O:3].[CH3:7][N:8]([CH2:10][CH2:11][CH2:12][CH2:13]CC(O)=O)[CH3:9].C(=O)=O>>[ClH:4].[CH3:7][N:8]([CH2:10][CH2:11][CH2:12][CH2:13][CH2:1][C:2]([Cl:4])=[O:3])[CH3:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 280Carbon DioxideHCID 65578Oxalyl chlorideHCID 140528476-(Dimethylamino)hexanoic acid

생성물 1

HCID 21475509HCID 21475509, 화합물

반응 조건

온도
40 °C

실험 절차

Into a 500 ml three-necked round-bottomed flask equipped with a reflux condenser, internal thermometer, mechanical stirrer, and argon inlet, is placed oxalyl chloride (398.67 g, 3.14 mol). Acid 2 (100 g, 0.63 mol) is added over 30 min while maintaining the reaction temperature at 40° C. As reaction takes place, CO2 and CO are swept away from the mixture with argon. After addition is complete, the mixture is stirred for 2 h while the reaction flask cools to room temperature. Excess oxalyl chloride is removed by rotary evaporation at 50° C. and then by Kugelrohr distillation at 50° C. (0.1 mm Hg) for 2 h. Isolated is 3, 118.98 g (88.5%) as an oil that solidifies on standing.

후처리

  1. customInto a 500 ml three-necked round-bottomed flask equipped with a reflux condenser
  2. customAs reaction
  3. additionAfter addition
  4. customcools to room temperature
  5. customExcess oxalyl chloride is removed by rotary evaporation at 50° C.
  6. distillationby Kugelrohr distillation at 50° C. (0.1 mm Hg) for 2 h
  7. customIsolated

출처 및 근거

ORD 기록
ord-4d3e00139f2d44f9adfe71477ae6b0c2
출처 데이터셋
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05561235

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