Water → 3-Bromo-6-propylpyridazine

HRID 1982120ノート

反応式

HRID 1982120 の反応式
[CH2:1]([C:4]1[CH:5]=[CH:6][C:7](=O)[NH:8][N:9]=1)[CH2:2][CH3:3].P(Br)(Br)([Br:13])=O.O.C(=O)([O-])O.[Na+]>C1(C)C=CC=CC=1>[Br:13][C:7]1[N:8]=[N:9][C:4]([CH2:1][CH2:2][CH3:3])=[CH:5][CH:6]=1

参加物

6

反応条件

温度
80 °C

実験手順

11.75 g of 6-propyl-3(2H)-pyridazinone were dissolved in 70 ml of absolute toluene while warming in a sulphonation flask under nitrogen, heated to 80° C. and treated dropwise while stirring well within 30 minutes with a solution of 24.4 g of phosphorus oxybromide in 24.4 g of absolute toluene. The mixture was subsequently stirred under reflux for a further 3 hours. After completion of the reaction, the mixture was poured into 200 ml of water and neutralized with solid sodium hydrogen carbonate. The phases were separated and the aqueous phase was back-extracted twice with 100 ml of tert.butyl methyl ether each time. The combined organic phases were washed with 100 ml of water and dried over sodium sulphate. After evaporation of the solvent, the dark brown crystalline residue (14.1 g) was sublimed at 40°-60° C. in a high vacuum, there being obtained 8.2 g (48%) of 3-bromo-6-propylpyridazine as white crystals of melting point 35°-36° C.

後処理

  1. temperaturewhile warming in a sulphonation flask under nitrogen
  2. additiontreated dropwise
  3. temperatureunder reflux for a further 3 hours
  4. customAfter completion of the reaction
  5. customThe phases were separated
  6. extractionthe aqueous phase was back-extracted twice with 100 ml of tert.butyl methyl ether each time
  7. washThe combined organic phases were washed with 100 ml of water
  8. dry with materialdried over sodium sulphate
  9. customAfter evaporation of the solvent
  10. customwas sublimed at 40°-60° C. in a high vacuum

出典と根拠

ORDレコード
ord-718d583c445040caa88924dcb877be55
出典データセット
uspto-grants-1986_06
特許番号
US04595521

反応ノート

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