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Chlorosuccinimide → 4-Methylthiophene-3-sulfonyl chloride

HRID 236525
ノート
印刷プレビュー

反応式

HRID 236525 の反応式
[CH3:1][C:2]1[C:3]([S:7]([O-:9])=[O:8])=[CH:4][S:5][CH:6]=1.[Li+].[Cl:11]N1C(=O)CCC1=O>O.CC(O)C>[CH3:1][C:2]1[C:3]([S:7]([Cl:11])(=[O:9])=[O:8])=[CH:4][S:5][CH:6]=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 2

HCID 31398ChlorosuccinimideHCID 23669555Lithium 4-methyl-3-thiophenesulfinate

生成物 1

HCID 232616744-Methylthiophene-3-sulfonyl chloride

試薬・触媒・溶媒 2

HCID 962Water溶媒2 回HCID 3776Isopropanol溶媒2 回

反応条件

温度
20 °C

実験手順

To 34 g of lithium 4-methyl-3-thiophenesulfinate in 220 ml of water cooled to 10° C. was added a suspension of 26.7 g of N-chlorosuccinimide in 80 ml of 2-propanol portionwise during 5 minutes. An additional 75 ml of 2-propanol was added to dissolve the reagents and the mixture was stirred for 70 minutes at 20° C. A large excess (1 liter) of water was then added and the mixture was extracted with methylene chloride 3 times. The methylene chloride portions were combined, dried over sodium sulfate and the solvent removed in vacuo to yield 4-methyl-3-thiophenesulfonyl chloride. This product was dissolved in 100 ml of tetrahydrofuran and 70 ml of concentrated aqueous ammonia was then added, and the mixture stirred overnight. Concentration of the resultant solution in vacuo and dilution of the residue with water yielded a solid which was filtered, washed with water and stirred with hot 1-chlorobutane, cooled and filtered to yield 14 g of the desired solid compound, m.p. 73°-85°.

後処理

  1. additionwas added
  2. dissolutionto dissolve the reagents
  3. extractionthe mixture was extracted with methylene chloride 3 times
  4. dry with materialdried over sodium sulfate
  5. customthe solvent removed in vacuo

出典と根拠

ORDレコード
ord-2bc43389863440bda78fe01356a6c85f
出典データセット
uspto-grants-1987_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04645529

反応ノート

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