Sodium Methoxide → HCID 68470880, compound

HRID 2380647Notes

Reaction equation

HRID 2380647 reaction equation
[C:1]([C@H:5]1[C@@H:11]([CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:10][C@H:9]2[N:19]([CH3:20])[C@@H:6]1[CH2:7][CH2:8]2)([O:3][CH3:4])=[O:2].C[O-].[Na+]>CO>[C:1]([C@@H:5]1[C@@H:11]([CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:10][C@H:9]2[N:19]([CH3:20])[C@@H:6]1[CH2:7][CH2:8]2)([O:3][CH3:4])=[O:2]

Participants

4

Procedure

To a solution of (1R,2S,3S)-2-carbomethoxy-3-benzyltropane (5.6 g, 20.5 mmol) in absolute methanol (100 ml) was added a solution of sodium methanolate in methanol (2M, 2 ml) and the mixture was refluxed for 16 hours. The reaction mixture was concentrated in vacuo and the remanescens was dissolved in diethyl ether and was washed with water. The organic phase was dried and concentrated in vacuo. The crude product was purified by column chromatography using a mixture of diethyl ether and pentane (1+1)+1% triethyl amine as eluent yielding (1R,2R,3S)-2-carbomethoxy-3-benzyltropane as an oil. By dissolution of this product in diethyl ether and subsequent addition of a solution of hydrochloric acid in diethyl ether the title compound precipitates as white crystals, m.p. 188°-190° C.

Workup

  1. temperaturethe mixture was refluxed for 16 hours
  2. concentrationThe reaction mixture was concentrated in vacuo
  3. dissolutionthe remanescens was dissolved in diethyl ether
  4. washwas washed with water
  5. customThe organic phase was dried
  6. concentrationconcentrated in vacuo
  7. customThe crude product was purified by column chromatography
  8. additiona mixture of diethyl ether and pentane (1+1)+1% triethyl amine as eluent

Sources & evidence

ORD record
ord-499d825289cc40c2b0112779be5c830b
Source dataset
uspto-grants-1994_11
Patent number
US05369113

Reaction notes

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