Sodium Acetate → HCID 12889060, compound

HRID 1278379Notes

Reaction equation

HRID 1278379 reaction equation
F[B-](F)(F)F.[CH2:6]([N+:8]1[S:9][C:10]([Cl:15])=[C:11]([Cl:14])[C:12]=1Cl)[CH3:7].C([O-])(=[O:18])C.[Na+]>>[Cl:14][C:11]1[C:12](=[O:18])[N:8]([CH2:6][CH3:7])[S:9][C:10]=1[Cl:15]

Participants

3

Reactant 2

HCID 517045Sodium AcetateHCID 128890412-Ethyl-3,4,5-trichloroisothiazolium tetrafluoroborate

Product 1

HCID 12889060HCID 12889060, compoundYield 45%

Procedure

2-Ethyl-3,4,5-trichloroisothiazolium tetrafluoroborate (14.5 g), 0.048 mol) was added in portions to 150 ml of a saturated sodium acetate solution. The aqueous phase was extracted with 3×50 ml of CH2Cl2. The combined extracts were dried (MgSO4), filtered and concentrated. The oil was distilled to yield 4.2 g (45%) 4,5-dichloro-2-ethyl-4-isothiazolin-3-one, bp 89-92 (0.1 mm).

Workup

  1. extractionThe aqueous phase was extracted with 3×50 ml of CH2Cl2
  2. dry with materialThe combined extracts were dried (MgSO4)
  3. filtrationfiltered
  4. concentrationconcentrated
  5. distillationThe oil was distilled

Sources & evidence

ORD record
ord-3498b53f46ce4659b559e0148885e8e4
Source dataset
uspto-grants-1981_07
Patent number
US04281136

Reaction notes

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