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Ethanolamine → 4-Hydroxy-3-methoxy-N,N-di(propan-2-yl)benzamide

HRID 2399960
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HRID 2399960 반응식
C([O:4][C:5]1[CH:19]=[CH:18][C:8]([C:9]([N:11]([CH:15]([CH3:17])[CH3:16])[CH:12]([CH3:14])[CH3:13])=[O:10])=[CH:7][C:6]=1[O:20][CH3:21])(=O)C.NCCO>>[OH:4][C:5]1[CH:19]=[CH:18][C:8]([C:9]([N:11]([CH:12]([CH3:13])[CH3:14])[CH:15]([CH3:17])[CH3:16])=[O:10])=[CH:7][C:6]=1[O:20][CH3:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 700EthanolamineHCID 18991745HCID 18991745, 화합물

생성물 1

HCID 217472594-Hydroxy-3-methoxy-N,N-di(propan-2-yl)benzamide

실험 절차

The combined filtrate (about 1260 mL), containing 4-acetoxy-3-methoxy-N,N-bis(1-methylethyl)-benzamide, is treated at room temperature under nitrogen while stirring with 2-aminoethanol (43.1 g, 42.6 mL) added dropwise over a 5 minute period. The reaction mixture is then heated at 78°-85° for 5 hours. The heat source is removed and water (400 mL) is added slowly over a period of 30 minutes. The stirred slurry is cooled to room temperature and stirring at room temperature is continued for 16 hours. The suspension is cooled to 5° C. and filtered. The resulting solid is washed with xylenes and dried in a vacuum oven at 40°-45° C. for 48 hours to obtain 4-hydroxy-3-methoxy-N,N-bis(1-methylethyl)benzamide; 1H-NMR (CDCl3): δ1.10-1.50 (m, 12H), 3.62-3.80 (m, 2H), 3.82 (s, 3H), 6.42-6.70 (m, 1H), 6.72-6.88 (m, 3H).

후처리

  1. additionis treated at room temperature under nitrogen
  • additionadded dropwise over a 5 minute period
  • temperatureThe reaction mixture is then heated at 78°-85° for 5 hours
  • customThe heat source is removed
  • additionwater (400 mL) is added slowly over a period of 30 minutes
  • temperatureThe suspension is cooled to 5° C.
  • filtrationfiltered
  • washThe resulting solid is washed with xylenes
  • customdried in a vacuum oven at 40°-45° C. for 48 hours
  • 출처 및 근거

    ORD 기록
    ord-e45ddc5020cd463186e910035c1a47cf
    출처 데이터셋
    uspto-grants-1995_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05451700

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