Phosgene → o-N,N-Diethylsulfamoylbenzenesulfonyl isocyanate

HRID 847656Notes

Reaction equation

HRID 847656 reaction equation
[CH2:1]([N:3]([CH2:17][CH3:18])[S:4]([C:7]1[C:8]([S:13]([NH2:16])(=[O:15])=[O:14])=[CH:9][CH:10]=[CH:11][CH:12]=1)(=[O:6])=[O:5])[CH3:2].C(N=[C:24]=[O:25])CCC.C(Cl)(Cl)=O>>[CH2:17]([N:3]([CH2:1][CH3:2])[S:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=1[S:13]([N:16]=[C:24]=[O:25])(=[O:14])=[O:15])(=[O:6])=[O:5])[CH3:18]

Participants

4

Reactant 3

HCID 6371PhosgeneHCID 8110Butyl isocyanateHCID 12819600N,N-diethyl-1,2-benzenedisulfonamide

Product 1

HCID 12819607o-N,N-Diethylsulfamoylbenzenesulfonyl isocyanate

Procedure

A solution of 13.2 g of N,N-diethyl-1,2-benzenedisulfonamide, 4.5 g of n-butylisocyanate, and 0.2 g of 1,4-diaza[2,2,2]bicyclooctane (DABCO) in 90 ml of mixed xylenes was heated to 135°. To this solution was added 3.3 ml of liquid phosgene at such a rate that the temperature was maintained between 125 and 135° (about 2 hours). The temperature was kept at 130° for 1/2 hour after the addition. The solution was cooled and filtered to remove a small amount of insoluble solid then concentrated at 60°-70° in-vacuo. The residue of o-N,N-diethylsulfamoylbenzenesulfonyl isocyanate was an oil weighing 16.8 g and was sufficiently pure for further reaction.

Workup

  1. temperaturewas maintained between 125 and 135° (about 2 hours)
  2. additionafter the addition
  3. temperatureThe solution was cooled
  4. filtrationfiltered
  5. customto remove a small amount of insoluble solid
  6. concentrationthen concentrated at 60°-70° in-vacuo
  7. customwas sufficiently pure for further reaction

Sources & evidence

ORD record
ord-a7eb8fd1093241beb677c6c5057b3077
Source dataset
uspto-grants-1981_10
Patent number
US04293330

Reaction notes

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