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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Chloroform → HCID 21951121, 화합물

HRID 1770745
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HRID 1770745 반응식
[NH2:1][C:2]([CH3:9])([CH3:8])[CH2:3][NH:4][CH2:5][CH2:6][OH:7].C(Cl)(Cl)Cl.[OH-:14].[Na+]>CC(C)=O>[OH:7][CH2:6][CH2:5][N:4]1[CH2:3][C:2]([CH3:9])([CH3:8])[NH:1][C:2]([CH3:9])([CH3:8])[C:3]1=[O:14]
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참가 물질

5

반응물 3

HCID 6212ChloroformHCID 14798Sodium HydroxideHCID 226840N1-(2-Hydroxyethyl)-2-methyl-1,2-propanediamine

생성물 1

HCID 21951121HCID 21951121, 화합물수율 15.9%

시약·촉매·용매 1

HCID 180Acetone용매

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온도
0 °C

실험 절차

To a solution of 2-((2-amino-2-methylpropyl)amino)ethanol (12 g, 91 mmol) in 90 mL of acetone was added chloroform (10.9 mL, 136 mmol) and the solution was cooled to 0° C. with an external ice bath. A solution of NaOH (50% by weight, 43.6 g, 545 mmol) was added slowly to the cold solution over several minutes and the resultant solution was stirred at 0° C. for 2 hours then allowed to warm to room temperature and stirred for an additional 18 hr. The crude reaction mixture was filtered to remove solids, washing with acetone, and the solution was concentrated to 20 g of a clear oil. A portion of the crude material was purified by a bulb-to-bulb distillation under reduced pressure to give 1.45 g of a clear oil, which was used directly in the next step without further purification. LRMS (ESI/APCI) m/z 201 [M+H]+.

후처리

  1. temperatureto warm to room temperature
  2. customThe crude reaction mixture
  3. filtrationwas filtered
  4. customto remove solids
  5. washwashing with acetone
  6. concentrationthe solution was concentrated to 20 g of a clear oil
  7. distillationA portion of the crude material was purified by a bulb-to-bulb distillation under reduced pressure

출처 및 근거

ORD 기록
ord-b8d9a6540c524b14afa817581abc9633
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09248117B2

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