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1,4-Naphthoquinone → HCID 19701080, 화합물

HRID 861923
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HRID 861923 반응식
[CH:1]1[CH:2]=[CH:3][C:4]2[C:11](=[O:12])[CH:10]=[CH:9][C:7](=[O:8])[C:5]=2[CH:6]=1.CN(C)[N:15]=[CH:16][C:17]([F:20])=[CH:18][CH3:19]>C(Cl)(Cl)Cl>[F:20][C:17]1[CH:16]=[N:15][C:9]2[C:7](=[O:8])[C:5]3[C:4]([C:11](=[O:12])[C:10]=2[C:18]=1[CH3:19])=[CH:3][CH:2]=[CH:1][CH:6]=3
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참가 물질

4

반응물 2

HCID 85301,4-NaphthoquinoneHCID 53662947HCID 53662947, 화합물

생성물 1

HCID 19701080HCID 19701080, 화합물수율 15%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

A solution of naphthoquinone (553 mg, 3.5 mmol) and 2-fluoro-2-butenal N,N-dimethylhydrazone was refluxed for 8 days in chloroform (15 ml.) After the solvent was evaporated at reduced pressure, the residue was chromatographed over silica gel column, eluting with petroleum ether-ethyl acetate (9:1) and yielded 63 mg (10%) of compound (I-k) and 90 mg (15%) of 3-fluoro-4-methyl-1-azaanthracen-9-10-dione. m.p. 190°-192° C. (CDCl3).

후처리

  1. customwas evaporated at reduced pressure
  2. customthe residue was chromatographed over silica gel column
  3. washeluting with petroleum ether-ethyl acetate (9:1)

출처 및 근거

ORD 기록
ord-c3f49e9feb5947f590c5adec72fb63b1
출처 데이터셋
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05716963

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