Iodine → HCID 10890716、化合物

HRID 2399609ノート

反応式

HRID 2399609 の反応式
[Cl:1]Cl.[F:3][C:4]([F:15])([F:14])[C:5]1[CH:13]=[CH:12][CH:11]=[CH:10][C:6]=1[CH:7]([Cl:9])[Cl:8].II>>[F:3][C:4]([F:14])([F:15])[C:5]1[CH:13]=[C:12]([Cl:1])[CH:11]=[CH:10][C:6]=1[CH:7]([Cl:9])[Cl:8]

参加物

4

反応条件

温度
60 °C

実験手順

A 500-ml four-necked round bottom flask equipped with thermometer, mechanical stirrer, Dimroth condenser and chlorine-introducing tube was charged with 570.0 g (2.5 mol) of o-trifluoromethylbenzalchloride, 11.5 g (2.5 mol %) of ferric chloride and 1.5 g (0.5 mol %) of iodine. Then, the reaction temperature was raised to 60° C. while the mixture was kept stirred. When the reaction temperature reached 60° C., chlorination was started by continuously introducing chlorine at a rate of 0.5 mol/hr. After the lapse of 2 hr, the reaction temperature was raised to 80° C., and then the reaction was continued for another 5 hr. After the 7-hr reaction, conversion was 97.0%. Then, the reaction liquid was put into a 1000-ml separating funnel, and washed two times with 500 ml of water. The mixed liquid was allowed to separate into two layers and the aqueous layer was removed. The organic phase was dried with magnesium sulfate, and then magnesium sulfate was removed by vacuum filtration. As the result, 634.2 g of 2-trifluoromethyl-4-chlorobenzalchloride (purity: 72.1%) was obtained. The yield of this product was 69.4%. The product was analyzed by gas chromatography, and the result is as follows.

後処理

  1. additionintroducing tube
  2. customreached 60° C.
  3. temperatureAfter the lapse of 2 hr, the reaction temperature was raised to 80° C.
  4. customAfter the 7-hr reaction, conversion
  5. customThen, the reaction liquid
  6. customseparating funnel
  7. washwashed two times with 500 ml of water
  8. customto separate into two layers
  9. customthe aqueous layer was removed
  10. dry with materialThe organic phase was dried with magnesium sulfate
  11. custommagnesium sulfate was removed by vacuum filtration

出典と根拠

ORDレコード
ord-c4c95d87af1e40ecbcbea710f958cb9b
出典データセット
uspto-grants-1995_09
特許番号
US05449831

反応ノート

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