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Acetyl chloride → 5,8-Dimethoxy-2-acetyl-3,4-dihydronaphthalene

HRID 897177
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HRID 897177 반응식
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[C:9]2[C:4]=1[CH2:5][CH2:6][CH:7]=[CH:8]2.[C:15](Cl)(=[O:17])[CH3:16].[Cl-].[Cl-].[Cl-].[Al+3]>>[C:15]([C:6]1[CH2:7][CH2:8][C:9]2[C:4](=[C:3]([O:2][CH3:1])[CH:12]=[CH:11][C:10]=2[O:13][CH3:14])[CH:5]=1)(=[O:17])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6367Acetyl chlorideHCID 2676515,8-Dimethoxy-1,2-dihydronaphthalene2회HCID 6451240Aluminum(III) Chloride2회

생성물 1

HCID 110642935,8-Dimethoxy-2-acetyl-3,4-dihydronaphthalene

실험 절차

In spite of the fact that in literature the attempts of acylating the compound II were reported as fruitless or non interesting because of the low yields, the 5,8-dimethoxy-3,4-dihydronaphthalene II is treated with acetyl chloride in the presence of an excess of aluminium trichloride, preferably 5-9 moles of aluminium trichloride for one mole of acyl chloride, at the temperature of −35°+25° C., preferably at 0° C. After the usual work-up and crystallisation with ethyl acetate, the product, 2-acetyl-5,8-dimethoxy-3,4-dihydronaphthalene is obtained in yields higher than 70%.

후처리

  1. customat the temperature of −35°+25° C.
  2. custompreferably at 0° C
  3. customAfter the usual work-up and crystallisation with ethyl acetate

출처 및 근거

ORD 기록
ord-72723d1aea884e46aebb7137c57153cc
출처 데이터셋
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06921841B2

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