Hydrochloric Acid → 4-Chlorotoluene-2-sulphonyl chloride

HRID 1285272Notes

Reaction equation

HRID 1285272 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:9])=[C:6](N)[CH:7]=1.[ClH:10].N([O-])=O.[Na+].[S:15](=[O:17])=[O:16]>O.C(O)(=O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:9])=[C:6]([S:15]([Cl:10])(=[O:17])=[O:16])[CH:7]=1

Participants

7

Conditions

Temperature
15 °C

Procedure

5-Chloro-2-methylbenzeneamine (1002 g) was added over 0.5 hr. to a stirred mixture of 5.5 L of concentrated hydrochloric acid and 1.5 L of acetic acid precooled to 0°-5° C. The resulting suspension was stirred 0.5 hr. A solution of 530 g of sodium nitrite in 0.9 L H2O was added over 1.0 hr. while maintaining the temperature at 0°-5° C. When addition was complete, the mixture was stirred 1.0 hr. at 0°-5° C. The diazonium salt was added to a stirred mixture of 6.0 L of acetic acid, 1000 g of sulfur dioxide and 16.8 g of cuprous chloride while maintaining the temperature about 15° C. When addition of the diazonium salt was complete, the mixture was stirred several hours at about 15° C. then allowed to warm to ambient temperature and stirred overnight. The reaction mixture was poured into ice-water, and the aqueous mixture was extracted with 12 L of methylene chloride. The organic solution was washed twice with 6 L water followed twice with 4 L of saturated sodium bicarbonate solution. The organic solution was dried over magnesium sulfate, filtered and the solvent evaporated in vacuo to give 1279.9 g of the title compound as a black oil.

Workup

  1. customprecooled to 0°-5° C
  2. temperaturewhile maintaining the temperature at 0°-5° C
  3. additionWhen addition
  4. stirringthe mixture was stirred 1.0 hr
  5. customat 0°-5° C
  6. stirringthe mixture was stirred several hours at about 15° C.
  7. temperatureto warm to ambient temperature
  8. stirringstirred overnight
  9. extractionthe aqueous mixture was extracted with 12 L of methylene chloride
  10. washThe organic solution was washed twice with 6 L water
  11. dry with materialThe organic solution was dried over magnesium sulfate
  12. filtrationfiltered
  13. customthe solvent evaporated in vacuo

Sources & evidence

ORD record
ord-5bc7bace478b432f9321c07ccb82cf1a
Source dataset
uspto-grants-1986_01
Patent number
US04566898

Reaction notes

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