Thionyl Chloride → 2,4-Dichloro-3-cyano-5-fluorobenzoyl chloride

HRID 49645ノート

反応式

HRID 49645 の反応式
S(Cl)(Cl)=O.[C:5]([C:7]1[C:8]([Cl:18])=[C:9]([CH:13]=[C:14]([F:17])[C:15]=1[Cl:16])[C:10](O)=[O:11])#[N:6].[ClH:19].S(=O)=O>N1C=CC=CC=1>[C:5]([C:7]1[C:8]([Cl:18])=[C:9]([CH:13]=[C:14]([F:17])[C:15]=1[Cl:16])[C:10]([Cl:19])=[O:11])#[N:6]

参加物

5

反応物 3

HCID 24386Thionyl ChlorideHCID 109005412,4-Dichloro-3-cyano-5-fluorobenzoic acidHCID 22338718Hydrogen chloride sulphur dioxide

生成物 1

HCID 143001312,4-Dichloro-3-cyano-5-fluorobenzoyl chloride収率 95.7%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

4100 ml of thionyl chloride and 41 ml of pyridine were introduced into a stirred apparatus fitted with metering device and gas outlet leading to a scrubber via a reflux condenser, and, at 20° C., 2050 g of 3-cyano-2,4-dichloro-5-fluorobenzoic acid (99.5% strength) were introduced at the rate of hydrogen chloride/sulphur dioxide evolution. At the end of the addition, the mixture was heated to reflux until the evolution of gas ceased. The mixture was then distilled. In the boiling range from 142 to 145° C./10 mbar, 2150 g (95.7% of theory) of 3-cyano-2,4-dichloro-5-fluorobenzoyl chloride were obtained (content according to GC: 98.0%).

後処理

  1. customfitted with metering device and gas outlet
  2. customleading to a scrubber via a reflux condenser
  3. additionAt the end of the addition
  4. temperaturethe mixture was heated
  5. temperatureto reflux until the evolution of gas
  6. distillationThe mixture was then distilled

出典と根拠

ORDレコード
ord-db20833cfd08478986e3edb813feb9a4
出典データセット
uspto-grants-2004_03
特許番号
US06706918B2

反応ノート

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