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Acetic Anhydride → 2,3-Dichloro-4-(2-phenylacryloyl)anisole

HRID 1578176
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인쇄 미리보기

반응식

HRID 1578176 반응식
[Cl:1][C:2]1[C:7]([Cl:8])=[C:6]([C:9](=[O:17])[CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:5]=[CH:4][C:3]=1[O:18][CH3:19].[C:20](OC(=O)C)(=O)C>>[Cl:1][C:2]1[C:7]([Cl:8])=[C:6]([C:9](=[O:17])[C:10]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH2:20])[CH:5]=[CH:4][C:3]=1[O:18][CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7918Acetic AnhydrideHCID 111301952,3-Dichloro-4-phenylacetylanisole

생성물 1

HCID 109248102,3-Dichloro-4-(2-phenylacryloyl)anisole수율 94%

실험 절차

Acetic anhydride (150 ml.) is added dropwise to a suspension of 2,3-dichloro-4-phenylacetylanisole (8.95 g., 30.3 mmol) in 15.3 ml. of N,N,N',N'-tetramethylenediaminomethane under an atmosphere of argon with ice-bath cooling. The reaction mixture stirred at 25° for 2 hrs. and poured into ice-water affords 11.9 g. of beige solid. An ethereal solution of the solid is washed with hydrochloric acid, water and then dried over magnesium sulfate. Removal of the solvent under reduced pressure provides 8.77 g. (94% yield) of 2,3-dichloro-4-(2-phenylacryloyl)anisole, m.p. 83.5°-86°.

후처리

  1. customaffords 11.9 g
  2. washAn ethereal solution of the solid is washed with hydrochloric acid, water
  • dry with materialdried over magnesium sulfate
  • customRemoval of the solvent under reduced pressure
  • customprovides 8.77 g
  • 출처 및 근거

    ORD 기록
    ord-a5a7d2c3afef49788d78af0da3e84da3
    출처 데이터셋
    uspto-grants-1981_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04291168

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