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Phthalic Anhydride → N-[3-(3,4-Dimethoxyphenyl)propyl]phthalimide

HRID 462113
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인쇄 미리보기

반응식

HRID 462113 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][CH2:12][CH2:13][NH2:14])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[C:15]1(=O)[O:20][C:18](=[O:19])[C:17]2=[CH:21][CH:22]=[CH:23][CH:24]=[C:16]12>C(O)(=O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][CH2:12][CH2:13][N:14]2[C:18](=[O:19])[C:17]3=[CH:21][CH:22]=[CH:23][CH:24]=[C:16]3[C:15]2=[O:20])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6811Phthalic AnhydrideHCID 22810533,4-Dimethoxybenzenepropanamine

생성물 1

HCID 21390569N-[3-(3,4-Dimethoxyphenyl)propyl]phthalimide

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

6.4 g of 3-(3,4-dimethoxyphenyl)-propylamine (0.03 moles) was refluxed with 5.47 g of phthalic anhydride (0.037 moles) in 70 ml of acetic acid for 2.5 hours. The solvent was then removed in the rotary evaporator. Recrystallization of the residue from 150 ml of ether gave 4.0 g of a first crop, m.p. 82°-85° and 7.0 g of a second crop, m.p. 81°-83°.

후처리

custom
The solvent was then removed in the rotary evaporator
  • customRecrystallization of the residue from 150 ml of ether
  • customgave 4.0 g of a first crop, m.p. 82°-85° and 7.0 g of a second crop, m.p. 81°-83°
  • 출처 및 근거

    ORD 기록
    ord-2f7ce66a3b0841688bec7cca222ca4c8
    출처 데이터셋
    uspto-grants-1977_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04065473

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