Hydrochloric Acid → 2,3-Dichlorobenzene-1-sulfonyl chloride

HRID 236516Notes

Reaction equation

HRID 236516 reaction equation
[Cl:1][C:2]1[C:8]([Cl:9])=[CH:7][CH:6]=[CH:5][C:3]=1N.[ClH:10].N([O-])=O.[Na+].[S:15](=[O:17])=[O:16]>C(O)(=O)C.O>[Cl:1][C:2]1[C:8]([Cl:9])=[CH:7][CH:6]=[CH:5][C:3]=1[S:15]([Cl:10])(=[O:17])=[O:16]

Participants

7

Conditions

Temperature
0 °C

Procedure

To a stirred solution of 70.0 g of 2,3-dichloroaniline in 51 mL of acetic acid was added 180 mL of concentrated hydrochloric acid portionwise. External cooling was used to maintain the temperature below 50° C. To this thick mixture at -5° C. was added a solution of 37.0 g of sodium nitrite in 80 mL of water dropwise at a rate that maintained the temperature below 50° C. After the addition was complete, the cloudy mixture was stirred at 0° C. for 10 minutes, and was then poured slowly into a suspension of 500 mL of acetic acid, 150 mL of sulfur dioxide and 10 g of cupric chloride dihydrate at 10°-20° C. Moderate gas evolution with excessive foaming occurred, but subsided after approximately ten minutes. This light brown mixture was stirred at ambient temperature for 1-1.5 hours and was then poured into 2 L of ice water with stirring. The resultant light brown precipitate was filtered, washed twice with 200 mL portions of water, and dried to yield 110 g of 2,3-dichlorobenzenesulfonyl chloride as a light brown solid, m.p. 56°-58° C., which was used without further purification; IR (nujol): 1375, 1175 cm-1.

Workup

  1. temperatureExternal cooling
  2. temperatureto maintain the temperature below 50° C
  3. temperaturethat maintained the temperature below 50° C
  4. additionAfter the addition
  5. waitsubsided after approximately ten minutes
  6. stirringThis light brown mixture was stirred at ambient temperature for 1-1.5 hours
  7. stirringwith stirring
  8. filtrationThe resultant light brown precipitate was filtered
  9. washwashed twice with 200 mL portions of water
  10. customdried

Sources & evidence

ORD record
ord-2270b8fa231c4123962660f4c8583c3f
Source dataset
uspto-grants-1987_02
Patent number
US04645527

Reaction notes

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