Chlorosuccinimide → 4-Methylthiophene-3-sulfonyl chloride

HRID 236525Notes

Reaction equation

HRID 236525 reaction equation
[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

Participants

5

Conditions

Temperature
20 °C

Procedure

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°.

Workup

  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

Sources & evidence

ORD record
ord-2bc43389863440bda78fe01356a6c85f
Source dataset
uspto-grants-1987_02
Patent number
US04645529

Reaction notes

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