Water → 2-(4-Nitro-1H-pyrazol-1-yl)ethan-1-ol

HRID 1968517Notes

Reaction equation

HRID 1968517 reaction equation
[N+:1]([C:4]1[CH:5]=[N:6][NH:7][CH:8]=1)([O-:3])=[O:2].[O:9]1[CH2:13][CH2:12]OC1=O.C(=O)([O-])[O-].[Cs+].[Cs+].O>CN(C)C=O.C(OCC)(=O)C>[N+:1]([C:4]1[CH:5]=[N:6][N:7]([CH2:12][CH2:13][OH:9])[CH:8]=1)([O-:3])=[O:2]

Participants

7

Conditions

Temperature
100 °C

Procedure

A solid mixture of 4-nitro-1H-pyrazole (1 g, 8.84 mmol), 1,3-dioxolan-2-one (3.89 g, 44.2 mmol) and cesium carbonate (2.88 g, 8.84 mmol) was suspended in 20 ml dimethylformamide and the resulting suspension was slowly heated to 100° C. overnight. The mixture was added to 100 ml water and 40 ml ethyl acetate; the separated aqueous layer was extracted with ethyl acetate (30 ml), and the combined organic layers were washed with brine (30 ml), dried with magnesium sulfate, filtered and concentrated. The residue was flash chromatographed (50 mm; 2% methanol/methylene chloride then 4% methanol/methylene chloride) to give the title compound with some residual DMF.

Workup

  1. extractionthe separated aqueous layer was extracted with ethyl acetate (30 ml)
  2. washthe combined organic layers were washed with brine (30 ml)
  3. dry with materialdried with magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customchromatographed (50 mm

Sources & evidence

ORD record
ord-a3b9a5837a2444289723ffe2c27776e4
Source dataset
uspto-grants-2013_04
Patent number
US08426408B2

Reaction notes

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