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Hydrogen Bromide → 5-Bromo-5-octylbarbituric acid

HRID 993071
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HRID 993071 반응식
[CH2:1]([CH:9]1[C:14](=[O:15])[NH:13][C:12](=[O:16])[NH:11][C:10]1=[O:17])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[BrH:18].BrBr>O>[Br:18][C:9]1([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[C:14](=[O:15])[NH:13][C:12](=[O:16])[NH:11][C:10]1=[O:17]
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참가 물질

5

반응물 3

HCID 260Hydrogen BromideHCID 24408BromineHCID 260794Barbituric acid, 5-octyl-

생성물 1

HCID 184088325-Bromo-5-octylbarbituric acid

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
2.5 °C

실험 절차

To a suspension of 5-octylbarbituric Acid (20 g) in 120 ml of water, cooled at 0-5° C., are added 12 ml of 48% hydrobromic acid and successively are dropped 4.72 ml of bromine. Ater 2 hours under stirring, the white solid which separated is recovered by filtration, washed with water and partitioned between 200 ml of diethyl ether and 100 ml of water. The aqueous phase is extracted with additional 50 ml of diethyl ether. The pooled organic phases are washed with 75 ml of saturated aqueous solution of sodium chloride, dried over sodium sulfate and concentrated to dryness. 25.8 g of the product as white solid are obtained.

후처리

  1. customthe white solid which separated
  2. filtrationis recovered by filtration
  3. washwashed with water
  4. custompartitioned between 200 ml of diethyl ether and 100 ml of water
  5. extractionThe aqueous phase is extracted with additional 50 ml of diethyl ether
  6. washThe pooled organic phases are washed with 75 ml of saturated aqueous solution of sodium chloride
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-2fc0ea8d86bb4c37af4ccdb34c80ccfb
출처 데이터셋
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06472396B1

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