Phosphorus pentachloride → (4-Cyanophenyl)methanesulfonyl chloride

HRID 1175004Notes

Reaction equation

HRID 1175004 reaction equation
[C:1]([C:3]1[CH:13]=[CH:12][C:6]([CH2:7][S:8](O)(=[O:10])=[O:9])=[CH:5][CH:4]=1)#[N:2].[Na].P(Cl)(Cl)(Cl)(Cl)[Cl:16]>P(Cl)(Cl)(Cl)=O>[C:1]([C:3]1[CH:13]=[CH:12][C:6]([CH2:7][S:8]([Cl:16])(=[O:10])=[O:9])=[CH:5][CH:4]=1)#[N:2]

Participants

5

Conditions

Temperature
80 °C

Procedure

5 g (22.83 mmol) of 4-cyanobenzylsulfonic acid, sodium salt, were moistened with approx. 20 ml of phosphoryl chloride after which 5.2 g (25.11 mmol) of PCl5 were added and the mixture was stirred for 15 min while being cooled with ice. The mixture was then heated at 80° C. for 4 h. After that, the mixture was poured onto ice and this fresh mixture was stirred vigorously for 30 min; the product then separated out on the ice as a white solid. After the ice had partially thawed, the mixture was filtered through a frit and the product/ice mixture which remained was washed several times with water. The crystals which remained were dried in vacuo and used directly for the next step in the synthesis.

Workup

  1. additionwere added
  2. temperaturewhile being cooled with ice
  3. additionAfter that, the mixture was poured onto ice
  4. stirringthis fresh mixture was stirred vigorously for 30 min
  5. customthe product then separated out on the ice as a white solid
  6. filtrationthe mixture was filtered through a frit
  7. washthe product/ice mixture which remained was washed several times with water
  8. customThe crystals which remained were dried in vacuo
  9. customused directly for the next step in the synthesis

Sources & evidence

ORD record
ord-bb2b7c635a604d35af31ad77439bbee2
Source dataset
uspto-grants-2010_11
Patent number
US07838560B2

Reaction notes

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