Diethyl Carbonate → HCID 89893995, compound

HRID 925426Notes

Reaction equation

HRID 925426 reaction equation
[CH2:1]([O:8][CH2:9][C@@H:10]1[CH2:12][O:11]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O.[NH2:14][NH2:15].C[O-].[Na+].[C:19](=[O:26])(OCC)OCC>>[NH2:14][N:15]1[CH2:12][C@@H:10]([CH2:9][O:8][CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[O:11][C:19]1=[O:26]

Participants

5

Conditions

Temperature
90 °C

Procedure

(S)-2-(Benzyloxymethyl)oxirane (2.5 g, 15.23 mmol) was added dropwise to hydrazine mono-hydrate (5.44 g, 107 mmol), previously heated at 90° C. The mixture was refluxed for 30 min, under stirring. The excess of hydrazine hydrate was evaporated under vacuum (8 mbar), at 60° C., for 6 h and then at room temperature, under vigorous magnetic stirring, for 18 h. The obtained sticky colourless oil was dissolved in dry methanol (5 mL) and a solution of sodium methoxide (0.5M in MeOH, 4.57 mL, 2.28 mmol) and then diethyl carbonate (2.16 g, 18.27 mmol) were added dropwise. The mixture was refluxed for 4 h 30 min. Solvent was evaporated and the crude purified by flash silica-gel chromatography (DCM/MeOH=75:1) affording the title compound as a yellow oil that solidified (white solid) on standing (2.074 g, 9.33 mmol). Yield=61%.

Workup

  1. temperatureThe mixture was refluxed for 30 min
  2. customThe excess of hydrazine hydrate was evaporated under vacuum (8 mbar), at 60° C., for 6 h
  3. dissolutionThe obtained sticky colourless oil was dissolved in dry methanol (5 mL)
  4. temperatureThe mixture was refluxed for 4 h 30 min
  5. customSolvent was evaporated
  6. customthe crude purified by flash silica-gel chromatography (DCM/MeOH=75:1)

Sources & evidence

ORD record
ord-c8791ff7bb164b13a60a6f894c1ea3c3
Source dataset
uspto-grants-2016_03
Patent number
US09284306B2

Reaction notes

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