Water → Pyridine-2-sulfonyl Chloride

HRID 1048736Notes

Reaction equation

HRID 1048736 reaction equation
S[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[Cl:8][O-].[Na+].O.[S:12](=[O:16])(=O)(O)[OH:13]>>[N:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[S:12]([Cl:8])(=[O:16])=[O:13]

Participants

5

Conditions

Temperature
-15 °C

Procedure

2-Mercaptopyridine (126 mg, 1 mmol) was dissolved in 5 mL of concentrated sulfuric acid to form a yellow solution, which was cooled to around −15° C. with a sodium chloride/ice (1/3) bath. Aqueous sodium hypochlorite solution (10-15%, 11 mL, 15-20 mmol) was added to the solution slowly enough to maintain the internal temperature of the reaction mixture below 10° C., with vigorous stirring. The reaction mixture was stirred at 0° C. for 1 hour and then 10 mL of water was added, which was then extracted with methylene chloride (20 mL×3). The combined organic phase was washed with water, dried with anhydrous magnesium sulfate, and then concentrated in vacuo. Pyridine-2-sulfonyl chloride (145 mg, 72%) was produced as a yellowish viscous liquid. 1H NMR (CDCl3): δ 7.684-7.729 (m, 1H), 8.043-8.143 (m, 2H), 8.84 (d, J=4.10 Hz, 1H).

Workup

  1. customto form a yellow solution, which
  2. temperatureto maintain the internal temperature of the reaction mixture below 10° C.
  3. extractionwhich was then extracted with methylene chloride (20 mL×3)
  4. washThe combined organic phase was washed with water
  5. dry with materialdried with anhydrous magnesium sulfate
  6. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-82cfaf7d864140c9ac87f0165426b304
Source dataset
uspto-grants-2016_07
Patent number
US09381260B2

Reaction notes

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