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Phosphorus oxychloride → 2,3-Dioxoindoline-5-sulfonyl chloride

HRID 571266
ノート
印刷プレビュー

反応式

HRID 571266 の反応式
O.O.[O:3]=[C:4]1[C:12](=[O:13])[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([S:14]([O-:17])(=O)=[O:15])[CH:10]=2)[NH:5]1.[Na+].O=P(Cl)(Cl)[Cl:21].S1(CCCC1)(=O)=O>O>[O:3]=[C:4]1[C:12](=[O:13])[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([S:14]([Cl:21])(=[O:17])=[O:15])[CH:10]=2)[NH:5]1
参加物反応条件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 24813Phosphorus oxychlorideHCID 31347SulfolaneHCID 51003678Isatin-5-sulfonic acid sodium salt dihydrate

生成物 1

HCID 159089472,3-Dioxoindoline-5-sulfonyl chloride収率 82%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
60 °C

実験手順

A suspension of sodium 2,3-dioxoindoline-5-sulfonate dihydrate (5.0 g, 17.53 mmol) and POCl3 (8.17 ml, 88 mmol) in sulfolane (25 ml, 264 mmol) was heated at 60° C. for 3 hours. The solution was cooled to 0° C. and water (60 ml) was added drop wise; the green precipitate was filtered and washed with a small amount of water. The solid was dissolved in ethyl acetate and washed three times with water; the organic phase was then dried over sodium sulfate and evaporated to give a crude solid that was purified by crystallization from hexane/ethyl acetate 1:1 to give 2,3-dioxoindoline-5-sulfonyl chloride (3.52 g, 14.33 mmol, 82% yield).

後処理

  1. temperatureThe solution was cooled to 0° C.
  2. filtrationthe green precipitate was filtered
  3. washwashed with a small amount of water
  4. dissolutionThe solid was dissolved in ethyl acetate
  5. washwashed three times with water
  6. dry with materialthe organic phase was then dried over sodium sulfate
  7. customevaporated
  8. customto give a crude solid that
  9. customwas purified by crystallization from hexane/ethyl acetate 1:1

出典と根拠

ORDレコード
ord-82bea943c6264cb68bb06a22af1cd06c
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09024027B2

反応ノート

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