Phosphorus oxychloride → Methyl (chlorosulfonyl)acetate

HRID 904348Notes

Reaction equation

HRID 904348 reaction equation
[CH3:1][O:2][C:3]([CH2:5][S:6]([O-:9])(=O)=[O:7])=[O:4].[Na+].P(Cl)(Cl)([Cl:13])=O>>[CH3:1][O:2][C:3]([CH2:5][S:6]([Cl:13])(=[O:9])=[O:7])=[O:4]

Participants

3

Procedure

The sodium methoxycarbonylmethylsulfonate salt was added in small portions to a stirred solution of 840 ml (9.14 mols) phosphorus oxychloride. The resulting mixture was then heated at 80°-100° C. for about 5 hours and allowed to cool overnight. The reaction mixture was filtered, the filtered solid was washed with dichloromethane and the filtrate distilled under reduced pressure to remove the dichloromethane and excess phosphorus oxychloride. The resulting oil residue was distilled through a short Vigreaux column to give 226.8 g (65.7% yield) of methoxycarbonylmethylsulfonyl chloride, as a yellow oil, b.p. 79°-80° C. (0.5 mm Hg).

Workup

  1. temperatureThe resulting mixture was then heated at 80°-100° C. for about 5 hours
  2. temperatureto cool overnight
  3. filtrationThe reaction mixture was filtered
  4. washthe filtered solid was washed with dichloromethane
  5. distillationthe filtrate distilled under reduced pressure
  6. customto remove the dichloromethane and excess phosphorus oxychloride
  7. distillationThe resulting oil residue was distilled through a short Vigreaux column

Sources & evidence

ORD record
ord-ce77dcce815b448bbc09bb04deca2eed
Source dataset
uspto-grants-1980_10
Patent number
US04230875

Reaction notes

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