Sulfuryl chloride → [(Chlorocarbonyl)oxy]methyl 2-methylpropanoate

HRID 1913545Notes

Reaction equation

HRID 1913545 reaction equation
[CH3:1][CH:2]([CH3:13])[C:3]([O:5][CH2:6][O:7][C:8](SCC)=[O:9])=[O:4].S(Cl)([Cl:17])(=O)=O>>[CH3:1][CH:2]([CH3:13])[C:3]([O:5][CH2:6][O:7][C:8]([Cl:17])=[O:9])=[O:4]

Participants

3

Procedure

The compound (400 mg) obtained in Step 2 of this Example was cooled to −30° C. Sulfuryl chloride (159 μL) was added thereto, and the mixture was stirred at the same temperature for 20 minutes. The mixture was in turn stirred for 20 minutes in an ice bath and further at room temperature for 1 hour. The solvent was distilled off under reduced pressure, and the residue was dried to obtain a crude product of the title compound.

Workup

  1. customwas cooled to −30° C
  2. stirringstirred for 20 minutes in an ice bath and further at room temperature for 1 hour
  3. distillationThe solvent was distilled off under reduced pressure
  4. customthe residue was dried

Sources & evidence

ORD record
ord-c58152f509424c4793a0f1ef193ef4f6
Source dataset
uspto-grants-2013_12
Patent number
US08609710B2

Reaction notes

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