Phosphorus pentachloride → (1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)methanesulfonyl chloride

HRID 1833545Notes

Reaction equation

HRID 1833545 reaction equation
[K+].[C:2]1(=[O:17])[N:6]([CH2:7][S:8]([O-])(=[O:10])=[O:9])[C:5](=[O:12])[C:4]2=[CH:13][CH:14]=[CH:15][CH:16]=[C:3]12.P(Cl)(Cl)(Cl)(Cl)[Cl:19]>C1C=CC=CC=1>[C:2]1(=[O:17])[N:6]([CH2:7][S:8]([Cl:19])(=[O:10])=[O:9])[C:5](=[O:12])[C:4]2=[CH:13][CH:14]=[CH:15][CH:16]=[C:3]12

Participants

4

Reactant 2

HCID 24819Phosphorus pentachloride2×HCID 88789710Phthalimidomethanesulfonic acid potassium salt

Product 1

HCID 21315191(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)methanesulfonyl chloride

Reagents, catalysts & solvents 1

HCID 241BenzeneSolvent

Procedure

To 41.7 g. (0.15 mol.) of phthalimidomethanesulfonic acid potassium salt in 220 ml. of dry benzene is added 22.5 g. (0.132 mol.) of phosphorus pentachloride. The reaction mixture is refluxed on a steam bath for one hour, then an additional 22.5 of phosphorus pentachloride is added and heating is continued for 1.5 hours. The reaction mixture is evaporated to dryness, crushed ice is added to the residue and the slurry is filtered. The product is washed with water to give phthalimidomethanesulfonyl chloride.

Workup

  1. temperatureThe reaction mixture is refluxed on a steam bath for one hour
  2. temperatureheating
  3. customThe reaction mixture is evaporated to dryness
  4. customcrushed ice
  5. additionis added to the residue
  6. filtrationthe slurry is filtered
  7. washThe product is washed with water

Sources & evidence

ORD record
ord-0a21e036ad85407a9e9e29944b8b59ec
Source dataset
uspto-grants-1978_01
Patent number
US04066762

Reaction notes

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