1-(5-(Hydroxymethyl)isoxazol-3-yl)ethanone → HCID 86669583, compound

HRID 1398540Notes

Reaction equation

HRID 1398540 reaction equation
[C:1]([Mg]Br)#[CH:2].[OH:5][CH2:6][C:7]1[O:11][N:10]=[C:9]([C:12](=[O:14])[CH3:13])[CH:8]=1>C1COCC1>[OH:5][CH2:6][C:7]1[O:11][N:10]=[C:9]([C:12]([OH:14])([C:1]#[CH:2])[CH3:13])[CH:8]=1

Participants

4

Reactant 2

HCID 105587091-(5-(Hydroxymethyl)isoxazol-3-yl)ethanoneHCID 178418486HCID 178418486, compound

Product 1

HCID 86669583HCID 86669583, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

To a solution of ethynylmagnesium bromide (0.5M in THF, 99 mL, 49.0 mmol) at 0° C. under N2 was added a solution of 1-[5-(hydroxymethyl)isoxazol-3-yl]ethanone (prepared according to Synthesis 2005, 20, 3541) (4.10 g, 29.0 mmol) in dry THF (25 mL) over 20 minutes. The reaction mixture was warmed to RT for 1.5 hr, quenched by dropwise addition of saturated aqueous ammonium chloride (20 mL) and concentrated in vacuo. After re-dissolving the residue in EtOAc (100 mL), the aqueous phase was removed, diluted with water to dissolve all suspended solids and washed with EtOAc (100 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated in vacuo to furnish the crude title compound as a red-brown syrup: 1H NMR (500 MHz, CDCl3) delta 1.88 (3H, s), 2.67 (1H, s), 4.77 (2H, s), 6.39 (1H, s); LC-MS: m/z=+167.9 (M+H)+. This compound, with LC-MS purity=88% UV, was used in the next step without further purification.

Workup

  1. customquenched by dropwise addition of saturated aqueous ammonium chloride (20 mL)
  2. concentrationconcentrated in vacuo
  3. dissolutionAfter re-dissolving the residue in EtOAc (100 mL)
  4. customthe aqueous phase was removed
  5. additiondiluted with water
  6. dissolutionto dissolve all suspended solids
  7. washwashed with EtOAc (100 mL)
  8. dry with materialThe combined organic extracts were dried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-41212ee8c6da47af9d57de6c7508aade
Source dataset
uspto-grants-2014_12
Patent number
US08901313B2

Reaction notes

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