Phosphorus oxychloride → HCID 178526406, compound

HRID 538119Notes

Reaction equation

HRID 538119 reaction equation
[Cl:1][C:2]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:5]2[NH:6][C:7](=O)[NH:8][C:4]=2[CH:3]=1.P(Cl)(Cl)([Cl:17])=O>>[Cl:17][C:7]1[NH:8][C:4]2[CH:3]=[C:2]([Cl:1])[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][C:5]=2[N:6]=1

Participants

3

Reactant 2

HCID 24813Phosphorus oxychlorideHCID 145662265-Chloro-1,3-dihydro-6-nitro-2H-benzimidazol-2-one

Product 1

HCID 178526406HCID 178526406, compoundYield 89%

Conditions

Temperature
85 °C

Procedure

To 5-chloro-6-nitro-1,3-dihydro-benzoimidazol-2-one (5.63 g, 26.35 mmol) was added phosphorus oxychloride (35 mL) and the reaction mixture was heated to 85° C. for 36 h. The reaction mixture was concentrated and the residue triturated with cold saturated aqueous sodium bicarbonate (to pH 8, 0.8 L). The resulting precipitate was collected and dried to yield the titled compound (5.43 g, 89% yield). MS (ESI/CI): mass calcd. for C7H3Cl2N3O2, 231.0; m/z found, 232.0 [M+H]+.

Workup

  1. concentrationThe reaction mixture was concentrated
  2. customthe residue triturated with cold saturated aqueous sodium bicarbonate (to pH 8, 0.8 L)
  3. customThe resulting precipitate was collected
  4. customdried

Sources & evidence

ORD record
ord-1798788d8cbb40c789ed14528a8377c5
Source dataset
uspto-grants-2014_10
Patent number
US08865713B2

Reaction notes

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