Sulfuric Acid → Hexachlorobutadiene

HRID 1680315

反応式

HRID 1680315 の反応式
S(=O)(=O)(O)O.[O:6]=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O.[Cl:20][C:21]1([Cl:29])[C:24]([Cl:25])=[C:23]([Cl:26])[C:22]1([Cl:28])[Cl:27]>>[Cl:20][C:21]1([Cl:29])[C:24](=[O:6])[C:23]([Cl:26])=[C:22]1[Cl:27].[Cl:20][C:21]1([Cl:29])[C:24]([Cl:25])=[C:23]([Cl:26])[C:22]1([Cl:28])[Cl:27].[Cl:20][C:21]([Cl:29])=[C:24]([Cl:25])[C:23]([Cl:26])=[C:22]([Cl:28])[Cl:27]

参加物

6

反応条件

温度
100 °C

実験手順

In a 1 liter flask, a mixture of 78 g of concentrated sulphuric acid and 78.5 g of phosphorus pentoxide was poured onto 100 g of 96% pure hexachlorocyclobutene [96 g (0.368 mole) of hexachlorocyclobutene; remainder hexachloro-1,3-butadiene], with stirring (molar ratio of hexachlorocyclobutene:sulphuric acid:phosphorus pentoxide=1:2:1). The mixture was heated at 100° C. for 3 hours. After cooling, the reaction mixture was poured onto ice, the organic phase was then separated immediately from the aqueous phase and the latter was extracted three times with petroleum ether. The petroleum ether solution and the organic phase were combined and dried with sodium sulphate, the petroleum ether was distilled under normal pressure and the residue was subjected to fractional distillation under 35 mbars. 43.6 g of tetrachlorocyclobutenone, 14.3 g of hexachlorocyclobutene and 3.6 g of hexachloro-1,3-butadiene were obtained. The selectivity of the reaction was 69.0% of theory with a conversion of 85% of theory.

後処理

  1. temperatureAfter cooling
  2. additionthe reaction mixture was poured onto ice
  3. customthe organic phase was then separated immediately from the aqueous phase
  4. extractionthe latter was extracted three times with petroleum ether
  5. dry with materialdried with sodium sulphate
  6. distillationthe petroleum ether was distilled under normal pressure
  7. distillationthe residue was subjected to fractional distillation under 35 mbars

出典と根拠

ORDレコード
ord-7320193863ee491a874bebdab0adc6d6
出典データセット
uspto-grants-1981_06
特許番号
US04272633

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