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Sulfuric Acid → 5-(2-Chloro-5-trifluoromethylphenoxy)-2-nitrobenzoic acid

HRID 358197
ノート
印刷プレビュー

反応式

HRID 358197 の反応式
[Cl:1][C:2]1[CH:17]=[CH:16][C:15]([C:18]([F:21])([F:20])[F:19])=[CH:14][C:3]=1[O:4][C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][CH:13]=1)[C:8]([OH:10])=[O:9].S(=O)(=O)(O)O.[N+:27]([O-])([O-:29])=[O:28].[K+]>ClCCCl>[Cl:1][C:2]1[CH:17]=[CH:16][C:15]([C:18]([F:20])([F:19])[F:21])=[CH:14][C:3]=1[O:4][C:5]1[CH:13]=[CH:12][C:11]([N+:27]([O-:29])=[O:28])=[C:7]([CH:6]=1)[C:8]([OH:10])=[O:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1118Sulfuric AcidHCID 24434Potassium NitrateHCID 193892503(2-Chloro-5-trifluoromethylphenoxy)benzoic acid

生成物 1

HCID 133898475-(2-Chloro-5-trifluoromethylphenoxy)-2-nitrobenzoic acid

試薬・触媒・溶媒 1

HCID 111,2-Dichloroethane溶媒

実験手順

The acid from (b) (2.0 g) was added to a mixture of concentrated sulphuric acid (15 ml) and 1,2-dichloroethane (10 ml) kept at 0°. Potassium nitrate (1.2 g) was then added in portions with stirring over a period of 30 minutes, keeping the temperature at 0°. The mixture was stirred for a further hour at 0° and then for 3 hours at room temperature. The mixture was then poured on to ice and extracted with ethyl acetate. The extract was washed with water, dried, and evaporated to give a dark gum. This was extracted several times with boiling cyclohexane. The residue crystallised on cooling and was identified as the required nitro-acid, with a melting point of 147°-148°.

後処理

  1. customkept at 0°
  2. customat 0°
  3. stirringThe mixture was stirred for a further hour at 0°
  4. waitfor 3 hours at room temperature
  5. additionThe mixture was then poured on to ice
  6. extractionextracted with ethyl acetate
  7. washThe extract was washed with water
  8. customdried
  9. customevaporated
  10. customto give a dark gum
  11. extractionThis was extracted several times with boiling cyclohexane
  12. customThe residue crystallised
  13. temperatureon cooling

出典と根拠

ORDレコード
ord-bbad34b5e6fc48d6a4d8d5c8aa8d6d48
出典データセット
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04465508

反応ノート

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