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Isopropylamine → 4-(4-methoxyphenyl)-N-(1-methylethyl)butylamine

HRID 2417991
노트
인쇄 미리보기

반응식

HRID 2417991 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][CH2:11][CH2:12]Br)=[CH:5][CH:4]=1.[CH:14]([NH2:17])([CH3:16])[CH3:15]>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][CH2:11][CH2:12][NH:17][CH:14]([CH3:16])[CH3:15])=[CH:5][CH:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6363IsopropylamineHCID 5781911-(4-Bromobutyl)-4-methoxybenzene

생성물 1

HCID 204469294-(4-methoxyphenyl)-N-(1-methylethyl)butylamine

반응 조건

온도
100 °C

실험 절차

A solution of (50 ml) isopropylamine and 4-(4-methoxyphenyl)butyl bromide (13.7 g) in a glass lined vessel was heated under nitrogen (initial pressure, 500 psi) for 12 hours at 100° C. The solvent was removed in vacuo and water (200 ml) was added to the residue. The solution was acidified with concentrated hydrochloric acid and the solution was extracted with ether. The extract was dried over potassium carbonate and the solvent was removed in vacuo. The residue, 4-(4-methoxyphenyl)-N-(1-methylethyl)butylamine, weighed 9.3 g (75%). The identity and purity (94.8%) of the product was determined by mass spectrum and gas chromatography.

후처리

  • customThe solvent was removed in vacuo and water (200 ml)
  • additionwas added to the residue
  • extractionthe solution was extracted with ether
  • dry with materialThe extract was dried over potassium carbonate
  • customthe solvent was removed in vacuo
  • 출처 및 근거

    ORD 기록
    ord-70a8b85604b7449ebbe788cd8acdafb8
    출처 데이터셋
    uspto-grants-1984_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04471116

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