Water → HCID 14304992, 화합물

HRID 477063노트

반응식

HRID 477063 반응식
C[O:2][C:3]1[CH:4]=[C:5]([CH:20]=[C:21]([O:25]C)[C:22]=1[O:23]C)[C:6]1[O:7][C:8]2[C:13]([C:14](=[O:19])[C:15]=1[C:16]([OH:18])=[O:17])=[CH:12][CH:11]=[CH:10][CH:9]=2.B(Br)(Br)Br.O>ClCCl>[OH:25][C:21]1[CH:20]=[C:5]([CH:4]=[C:3]([OH:2])[C:22]=1[OH:23])[C:6]1[O:7][C:8]2[C:13]([C:14](=[O:19])[C:15]=1[C:16]([OH:18])=[O:17])=[CH:12][CH:11]=[CH:10][CH:9]=2

참가 물질

5

반응물 3

HCID 962Water2회HCID 25134Boron tribromideHCID 143049774-Oxo-2-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-3-carboxylic acid

생성물 1

HCID 14304992HCID 14304992, 화합물수율 85%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

4.0 g of 3',4',5'-trimethoxyflavone-3-carboxylic acid were added to 200 ml of absolute dichloromethane and reacted with 82 ml of a 1 molar boron tribromide solution in absolute dichloromethane under a nitrogen atmosphere at 0° C. The reaction mixture was stirred for twelve hours during which it was allowed to warm to room temperature. Then, for working up, water was carefully added under ice cooling, then made up to twice the volume with water and intensively stirred. The resulting 3',4',5'-trihydroxyflavone-3-carboxylic acid precipitated and was filtered out. The filter cake was washed with water several times and recrystallized from methanol. 3 g of pure 3',4',5'-trihydroxyflavone-3-carboxylic acid were obtained.

후처리

  1. stirringintensively stirred
  2. customThe resulting 3',4',5'-trihydroxyflavone-3-carboxylic acid precipitated
  3. filtrationwas filtered out
  4. washThe filter cake was washed with water several times
  5. customrecrystallized from methanol

출처 및 근거

ORD 기록
ord-ba6229479aa04f53b7f9cc7803868a3c
출처 데이터셋
uspto-grants-1989_12
특허 번호
US04886806

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