Methanesulfonyl chloride → HCID 10878028, compound

HRID 2295995Notes

Reaction equation

HRID 2295995 reaction equation
[CH3:1][C:2]([CH3:8])([CH2:6][OH:7])[C:3](=[O:5])[CH3:4].[CH3:9][S:10](Cl)(=[O:12])=[O:11]>N1C=CC=CC=1.C(Cl)Cl>[CH3:9][S:10]([O:7][CH2:6][C:2]([CH3:8])([CH3:1])[C:3](=[O:5])[CH3:4])(=[O:12])=[O:11]

Participants

5

Reactant 2

HCID 31297Methanesulfonyl chlorideHCID 111943184-Hydroxy-3,3-dimethylbutan-2-one

Product 1

HCID 10878028HCID 10878028, compoundYield 86%

Reagents, catalysts & solvents 2

HCID 1049PyridineSolventHCID 6344DichloromethaneSolvent

Procedure

232 g (2 moles) of 3,3-dimethyl-4-hydroxy-2-butanone (for the preparation, see Beilstein H 1 E III 3239, IV 4030 and Bull. Soc. Chim.France 1964, 2849) were reacted with 229 g (2 moles) of methanesulphonyl chloride in 700 ml of absolute pyridine at 0° to 5° C. After leaving the mixture to stand at 20° C. for 12 hours, it was diluted with methylene chloride and extracted by shaking with ice-water. The organic phase was dried, and freed from the solvent in vacuo, and the residue was fractionated over a column. 332 g (that is to say 86% of theory) of 2,2-dimethyl-3-oxo-butyl methanesulphonate were isolated at a boiling point0.12 of 106° to 120° C. ##STR12##

Workup

  1. customAfter leaving the mixture
  2. extractionextracted
  3. customThe organic phase was dried

Sources & evidence

ORD record
ord-5deadf8cb5984069915c2778a4756d9d
Source dataset
uspto-grants-1984_01
Patent number
US04427672

Reaction notes

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