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Diethyl Ether →

HRID 620757
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HRID 620757 반응식
[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]#[N:12])=[CH:6][C:5]=1[O:13][CH3:14])[CH3:2].[C:15](OC(=O)C)(=[O:17])[CH3:16].[Cl:22]([OH:26])(=[O:25])(=[O:24])=[O:23].[CH2:27]([O:29]CC)[CH3:28]>>[Cl:22]([O-:26])(=[O:25])(=[O:24])=[O:23].[C:15]([NH:12][C:11]1[O:29][CH2+:27]([CH3:28])[C:8]2[CH:9]=[C:4]([O:3][CH2:1][CH3:2])[C:5]([O:13][CH3:14])=[CH:6][C:7]=2[CH:10]=1)(=[O:17])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 4

HCID 3283Diethyl EtherHCID 7918Acetic AnhydrideHCID 24247Perchloric AcidHCID 38639514-Ethoxy-3-Methoxyphenylacetonitrile

생성물 0

아직 생성물 데이터가 없습니다.

실험 절차

To an ice-cooled and stirred solution of 25 grams 4-ethoxy-3-methoxyphenylacetonitrile (0.13 mmol) in 74 ml acetic anhydride (0.785 mol) was slowly added perchloric acid (70%, 11.7 N, 15.5 ml, 0.182 mol) over a 15 minute period. The dark reaction mixture slowly became a yellow slurry and was stirred at room temperature for 42 hours. The mixture was diluted with 200 ml diethyl ether and a crystalline yellow solid was isolated by filtration, washed with diethyl ether and dried in vacuo to provide 47.3 grams of Compound 8d (100% yield) having a melting point of 188°-189° C. (with decomposition).

후처리

  1. custom
over a 15 minute
  • customThe dark reaction mixture
  • customa crystalline yellow solid was isolated by filtration
  • washwashed with diethyl ether
  • customdried in vacuo
  • 출처 및 근거

    ORD 기록
    ord-ff4e33adafad47d1a4a2746b694a7fab
    출처 데이터셋
    uspto-grants-1989_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04822800

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