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Hydrogen Bromide → 4-Fluorophenylglyoxal hydrate

HRID 1003724
ノート
印刷プレビュー

反応式

HRID 1003724 の反応式
[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][C:7]([F:10])=[CH:6][CH:5]=1)=[O:3].Br.CS(C)=[O:14]>>[OH2:3].[F:10][C:7]1[CH:8]=[CH:9][C:4]([C:2]([CH:1]=[O:14])=[O:3])=[CH:5][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 260Hydrogen BromideHCID 679Dimethyl SulfoxideHCID 98284'-Fluoroacetophenone

生成物 1

HCID 27374704-Fluorophenylglyoxal hydrate収率 73%

実験手順

4-Fluoroacetophenone (27.6 g, 0.2 moles) was dissolved in dimethylsulfoxide (140 ml). 48% Hydrobromic acid (101.1 g, 68.0 ml, 0.6 moles) was added over 20 minutes. The resulting solution was aged at 55-60° C. for 22 hours. The mixture was cooled to room temperature and partitioned between water (1.0 liters) and ethyl acetate (250 ml). The aqueous phase was extracted with ethyl acetate (2×250 ml). The combined ethyl acetate extracts were filtered and solvent switched to toluene at 60° C. under reduced pressure. The solution was diluted to 200 ml with toluene, and water (10 ml) was added. The resulting slurry was stirred at room temperature for 18 hours then at 0° C. for 1 hour. The product was collected by filtration and washed with cold toluene (50 ml). The solid was sucked down on the filter for 30 minutes and air dried to constant weight to afford 4-fluorophenylglyoxal hydrate (24.8 g) as a white solid in 73% yield.

後処理

  1. custompartitioned between water (1.0 liters) and ethyl acetate (250 ml)
  2. extractionThe aqueous phase was extracted with ethyl acetate (2×250 ml)
  3. filtrationThe combined ethyl acetate extracts were filtered
  4. customswitched to toluene at 60° C. under reduced pressure
  5. additionThe solution was diluted to 200 ml with toluene, and water (10 ml)
  6. additionwas added
  7. waitat 0° C. for 1 hour
  8. filtrationThe product was collected by filtration
  9. washwashed with cold toluene (50 ml)
  10. filtrationfilter for 30 minutes
  11. customair dried to constant weight

出典と根拠

ORDレコード
ord-72273756a42c4f77a9cf7530c993b8a1
出典データセット
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06046325

反応ノート

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