Réaction #1772040

ord-11dbc9b2c75f4bc8bd10a7c394abff87

Équation de réaction

COC(=O)NC(C(=O)OC)C1COC1
methyl 2-(methoxycarbonylamino)-2-(oxetan-3-yl)acetate
O.[Li+].[OH-]
lithium hydroxide monohydrate
O=S(=O)(O)O
sulfuric acid
[Li+].[OH-]
LiOH
COC(=O)NC(C(=O)[O-])C1COC1.[Li+]
lithium 2-(methoxycarbonylamino)-2-(oxetan-3-yl)acetate
Rendement 114.6%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.STIRRINGto stir overnight at which time TLC
  2. 2
    ConcentrationConcentrated in vacuo

Mode opératoire

To methyl 2-(methoxycarbonylamino)-2-(oxetan-3-yl)acetate (50 mg, 0.246 mmol) in THF (2 mL) and water (0.5 mL) was added lithium hydroxide monohydrate (10.33 mg, 0.246 mmol). The resultant solution was allowed to stir overnite at ambient temperature. TLC (1:1 EA/Hex; Hanessian stain [1 g Ce(NH4)2SO4, 6 g ammonium molybdate, 6 ml sulfuric acid, and 100 ml water]) indicated ˜10% starting material remaining. Added an additional 3 mg LiOH and allowed to stir overnight at which time TLC showed no starting material remaining. Concentrated in vacuo and placed on high vac overnite providing 55 mg lithium 2-(methoxycarbonylamino)-2-(oxetan-3-yl)acetate as a colorless solid. 1H NMR (500 MHz, MeOD) δ ppm 3.39-3.47 (m, 1H) 3.67 (s, 3H) 4.28 (d, J=7.93 Hz, 1H) 4.64 (t, J=6.26 Hz, 1H) 4.68 (t, J=7.02 Hz, 1H) 4.73 (d, J=7.63 Hz, 2H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08147818B2uspto-grants-2012_04