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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hexylamine → 2-Hexylamino-3-methoxypropionaldehyde

HRID 2083605
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반응식

HRID 2083605 반응식
Cl[CH:2]([CH2:5][O:6][CH3:7])[CH:3]=[O:4].[CH2:8]([NH2:14])[CH2:9][CH2:10][CH2:11][CH2:12][CH3:13]>C1(C)C=CC=CC=1>[CH2:8]([NH:14][CH:2]([CH2:5][O:6][CH3:7])[CH:3]=[O:4])[CH2:9][CH2:10][CH2:11][CH2:12][CH3:13]
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참가 물질

4

반응물 2

HCID 8102HexylamineHCID 145297052-Chloro-3-methoxypropionaldehyde

생성물 1

HCID 203570292-Hexylamino-3-methoxypropionaldehyde

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

The dimethyl acetal of 2-chloro-3-methoxypropionaldehyde (0.1 mole) and toluene (75 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. Hexylamine (0.22 mole) is added to the reaction mixture with stirring at room temperature. Stirring is continued fo a period of about 15 minutes. After this time the reaction mixture is heated at reflux for a period of about 1 hour. The reaction mixture is then cooled to room temperature and filtered. The filtrate is stripped of toluene and unreacted starting material under reduced pressure to yield the desired product the dimethyl acetal of 2-hexylamino-3-methoxypropionaldehyde as the residue.

후처리

  1. customequipped with a mechanical stirrer
  2. temperaturethermometer and reflux condenser
  3. stirringStirring
  4. temperatureAfter this time the reaction mixture is heated
  5. temperatureat reflux for a period of about 1 hour
  6. temperatureThe reaction mixture is then cooled to room temperature
  7. filtrationfiltered

출처 및 근거

ORD 기록
ord-314d38966e6b4b97a94a87f1b612027c
출처 데이터셋
uspto-grants-1978_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04086238

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