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Salicylamide → HCID 776579, 화합물

HRID 1637308
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HRID 1637308 반응식
[C:1]([NH2:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].[CH3:11][O:12][C:13]1[CH:21]=[CH:20][C:16]([C:17](Cl)=O)=[CH:15][CH:14]=1>C(O)(C)C>[CH3:11][O:12][C:13]1[CH:21]=[CH:20][C:16]([C:17]2[O:4][C:3]3[CH:5]=[CH:6][CH:7]=[CH:8][C:2]=3[C:1](=[O:9])[N:10]=2)=[CH:15][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5147SalicylamideHCID 7477p-Anisoyl chloride

생성물 1

HCID 776579HCID 776579, 화합물수율 80.6%

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

6.85 g (50 mmol) of salicylic acid amide are added, dropwise, to 18.1 g of p-methoxybenzoyl chloride and the mixture is heated to 150° C. The mixture is then stirred for 30 minutes at this temperature. After cooling, the honey-like mass is stirred with 100 ml of isopropanol, the precipitated solid filtered off and dried to yield 10.2 g of 2-(4-methoxyphenyl)-4H-1,3-benzoxazin-4-one as a white solid melting at 175-178° C. and having the following elemental analysis:

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • temperatureAfter cooling
  • filtrationthe precipitated solid filtered off
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-bbbbae17ac964de7a7498d5638383439
    출처 데이터셋
    uspto-grants-2000_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06040443

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