Triphenylphosphine → (E)-3-Methylbut-1-ene-1-sulfonyl chloride

HRID 333079Notes

Reaction equation

HRID 333079 reaction equation
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[S:20]([Cl:24])(Cl)(=[O:22])=[O:21].[CH3:25][CH:26]([CH3:33])/[CH:27]=[CH:28]/S([O-])(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC>ClCCl>[CH3:25][CH:26]([CH3:33])/[CH:27]=[CH:28]/[S:20]([Cl:24])(=[O:22])=[O:21]

Participants

5

Procedure

To a solution of triphenylphosphine (1.055 g, 4.02 mmol) in dichloromethane (50 ml) under a nitrogen atmosphere was added at 0° C. sulfuryl dichloride (0.359 ml, 4.42 mmol). The mixture was stirred at 0° C. for 15 minutes after which a solution of tetrabutylammonium (E)-3-methylbut-1-ene-1-sulfonate (1.25 g of Step C) in dichloromethane (10 ml) was added dropwise. The reaction mixture was stirred at room temperature for 5 h after which the mixture was concentrated under reduced pressure. The residue was taken up in diethylether and filtered over a glass filter to remove triphenylphosphinoxide. The filtrate was concentrated under reduced pressure to yield 102 mg of a brown oil which was used directly in the next step.

Workup

  1. additionwas added dropwise
  2. concentrationwas concentrated under reduced pressure
  3. filtrationfiltered over a glass
  4. filtrationfilter
  5. customto remove triphenylphosphinoxide
  6. concentrationThe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-af8749051f324d00be2b35ca27fdb808
Source dataset
uspto-grants-2014_11
Patent number
US08877934B2

Reaction notes

Loading…