Water → Florfenicol phthalate

HRID 2116677노트

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HRID 2116677 반응식
[CH3:1][S:2]([C:5]1[CH:6]=[CH:7][C:8]([C@@H:11]([OH:21])[C@H:12]([NH:15][C:16]([CH:18]([Cl:20])[Cl:19])=[O:17])[CH2:13][F:14])=[CH:9][CH:10]=1)(=[O:4])=[O:3].[C:22]1(=[O:32])[O:27][C:25](=[O:26])[C:24]2=[CH:28][CH:29]=[CH:30][CH:31]=[C:23]12.C(N(CC)CC)C.[OH2:40]>O1CCOCC1.ClCCl>[CH3:1][S:2]([C:5]1[CH:6]=[CH:7][C:8]([C@@H:11]([OH:21])[C@H:12]([NH:15][C:16]([CH:18]([Cl:20])[Cl:19])=[O:17])[CH2:13][F:14])=[CH:9][CH:10]=1)(=[O:4])=[O:3].[C:25]([O-:27])(=[O:26])[C:24]1[C:23](=[CH:31][CH:30]=[CH:29][CH:28]=1)[C:22]([O-:32])=[O:40]

참가 물질

7

실험 절차

3.9 g of florfenicol, 3.6 g of phthalic anhydride and 7.2 ml of triethyl amine in 36 ml of dioxane were taken in a 100 ml round bottom flask equipped with a magnetic stir bar and a drying tube. The reaction mixture was stirred at room temperature for 6 hours. After 6 hours, the contents were poured into 300 ml of cold water. The resulting gummy solid was dissolved in dichloromethane and washed thoroughly with saturated bicarbonate several times followed by water. The organic layer was dried over anhydrous sodium sulfate and concentrated over roto-evaporator. The semisolid obtained was recrystallized in a mixture of ethylacetate and hexane to obtain a solid product of 4.2 grams.

후처리

  1. customequipped with a magnetic stir bar and a drying tube
  2. waitAfter 6 hours
  3. washwashed thoroughly with saturated bicarbonate several times
  4. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  5. concentrationconcentrated over roto-evaporator
  6. customThe semisolid obtained
  7. customwas recrystallized in a mixture of ethylacetate and hexane
  8. customto obtain a solid product of 4.2 grams

출처 및 근거

ORD 기록
ord-157d98fd73714c4490988a776edf3900
출처 데이터셋
uspto-grants-2008_10
특허 번호
US07439268B2

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