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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-Amino-2-propanol → 2-Hydroxy-n-(2-hydroxypropyl)propanamide

HRID 1748965
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HRID 1748965 반응식
[NH2:1][CH2:2][CH:3]([OH:5])[CH3:4].[C:6]([O:11]CC)(=O)[CH:7]([CH3:9])[OH:8]>C(O)C>[C:6]([NH:1][CH2:2][CH:3]([OH:5])[CH3:4])(=[O:11])[CH:7]([CH3:9])[OH:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 41-Amino-2-propanolHCID 7344Ethyl Lactate

생성물 1

HCID 2213312-Hydroxy-n-(2-hydroxypropyl)propanamide

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

22.6 g 1-amino-2-propanol was added to 56.5 g ethyl lactate at room temperature. The mixture was heated to reflux and stirred for 4 hours. The reaction mixture was cooled and left to stand overnight at room temperature. The following day the ethanol formed and the excess of ethyl lactate were removed from the reaction mixture by distillation, using a 20 cm vigreux column 43 g of N-lactoyl 1-amino-2-propanol (pale brown viscous liquid) was collected as residue and cooled to room temperature. The purity of the obtained product was confirmed by NMR analysis.

후처리

  1. temperatureThe mixture was heated
  2. temperatureto reflux
  3. temperatureThe reaction mixture was cooled
  4. waitleft
  5. waitto stand overnight at room temperature
  6. customthe excess of ethyl lactate were removed from the reaction mixture by distillation
  7. customwas collected as residue

출처 및 근거

ORD 기록
ord-45730e5939bc40feab054eb051fe38e4
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09155329B2

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