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Sulfuric Acid → 4-Chlorophthalic acid

HRID 1658538
ノート
印刷プレビュー

反応式

HRID 1658538 の反応式
[Na].[Cl:2][C:3]1[CH:4]=[C:5]([C:12]([O-:14])=[O:13])[C:6](=[CH:10][CH:11]=1)[C:7]([O-:9])=[O:8].S(=O)(=O)(O)O>O>[Cl:2][C:3]1[CH:4]=[C:5]([C:12]([OH:14])=[O:13])[C:6](=[CH:10][CH:11]=1)[C:7]([OH:9])=[O:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 1118Sulfuric AcidHCID 86733574CID 86733574

生成物 1

HCID 69644-Chlorophthalic acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a suspension of 750 g of monosodium-4-chlorophthalate and 1200 ml water was added 120 ml conc. sulfuric acid. The resulting brown solution was extracted with three 400 ml portions of ether. The combined extracts were treated with carbon black, filtered and the ether distilled. The 4-chlorophthalic acid obtained was dehydrated by heating to 170°C for two hours to give 548 g of anhydride. To a solution of the anhydride in 2250 ml of xylene was added 279 g of aniline diluted with an equal weight of xylene. The solution was refluxed for 16 hours and the water formed was collected in a Dean-Stark trap. After treatment with carbon black the hot xylene solution was cooled to 5°C to give 475 g of crude 4-chloro-N-phenyl phthalimide. Recrystallization from 2000 ml toluene, twice, provided 364 g of 92% pure imide.

後処理

  1. extractionThe resulting brown solution was extracted with three 400 ml portions of ether
  2. additionThe combined extracts were treated with carbon black
  3. filtrationfiltered
  4. distillationthe ether distilled

出典と根拠

ORDレコード
ord-f546b1a78b8e4caf9c0bb7d3f88d9e10
出典データセット
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03965125

反応ノート

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