Hydrochloric Acid → 1-(1,5-Diethyl-1H-pyrazol-3-yl)ethanone

HRID 1452088Notes

Reaction equation

HRID 1452088 reaction equation
CON(C)[C:4]([C:6]1[CH:10]=[C:9]([CH2:11][CH3:12])[N:8]([CH2:13][CH3:14])[N:7]=1)=[O:5].[CH3:16][Mg]Br.C(O)C.Cl>O1CCCC1.CCOCC.CCOC(C)=O.O>[C:4]([C:6]1[CH:10]=[C:9]([CH2:11][CH3:12])[N:8]([CH2:13][CH3:14])[N:7]=1)(=[O:5])[CH3:16]

Participants

9

Procedure

N-Methoxy-N-methyl-1,5-diethylpyrazole-3-carboxamide (10.1 g) in dry tetrahydrofuran (180 ml) was cooled in an ice-bath and treated with a 3.0M solution of methylmagnesium bromide in ether (20.68 ml) added dropwise over 10 minutes. After stirring for 1 hour the mixture was treated with a mixture of ethanol (5 ml) and 5M aqueous HCl (1 ml). The mixture was then diluted with EtOAc and water. The organic phase was separated and the aqueous phase extracted twice with EtOAc. The combined organic extracts were dried over MgSO4 and evaporated in vacuo to leave an oil which was chromatographed on silica gel, loading in dichloromethane, and eluting with ethyl acetate/hexane mixtures to give, after evaporation of the requisite fractions, the product as an oil (8.08 g). δ(CDCl3) 1.29 (3H, t, J 7 Hz), 1.45 (3H, t, J 7 Hz), 2.55 (3H, s), 2.64 (2H, q, J 7 Hz), 4.14 (2H, q, J 7 Hz,), 6.55 (1H,s) ppm.

Workup

  1. additionadded dropwise over 10 minutes
  2. customThe organic phase was separated
  3. extractionthe aqueous phase extracted twice with EtOAc
  4. dry with materialThe combined organic extracts were dried over MgSO4
  5. customevaporated in vacuo
  6. customto leave an oil which
  7. customwas chromatographed on silica gel, loading in dichloromethane
  8. washeluting with ethyl acetate/hexane
  9. customto give
  10. customafter evaporation of the requisite fractions

Sources & evidence

ORD record
ord-da79723863314482a21ba1b1e160cfda
Source dataset
uspto-grants-1997_02
Patent number
US05606051

Reaction notes

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