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Triphenylphosphane dibromide → HCID 59814839, 화합물

HRID 2116657
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HRID 2116657 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:17]3[C:12](=[C:13]([CH3:19])[C:14](O)=[CH:15][CH:16]=3)[O:11][C:10](=[O:20])[CH:9]=2)=[CH:4][CH:3]=1.[Br-:21].[Br-].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>ClCCl>[Br:21][C:14]1[C:13]([CH3:19])=[C:12]2[C:17]([C:8]([C:5]3[CH:6]=[CH:7][C:2]([F:1])=[CH:3][CH:4]=3)=[CH:9][C:10](=[O:20])[O:11]2)=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12890784Triphenylphosphane dibromideHCID 59814860HCID 59814860, 화합물

생성물 1

HCID 59814839HCID 59814839, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

4-(4-fluorophenyl)-7-hydroxy-8-methyl-2-H-chromen-2-one, (4.47 g, 16.5 mol) and triphenylphosphine dibromide (7.68 g, 18.2 mmol) were heated in a sand bath at 320-350° C. for 0.5 h. The cooled mixture was dissolved in dichloromethane, silica gel was added and the mixture was evaporated. Chromatography on silica gel (hexane/EtOAC; 90:10), gave the title compound.

후처리

addition
silica gel was added
  • customthe mixture was evaporated
  • 출처 및 근거

    ORD 기록
    ord-e6138d3851de4ebbb2c59673a1074aae
    출처 데이터셋
    uspto-grants-2008_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07439260B2

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