Hydrochloric Acid → trans Ethyl 1-ethoxycarbonyl-3-[2-(benzyloxymethoxy)-ethyl]-pyrrolidine-2-carboxylate

HRID 1587341Notes

Reaction equation

HRID 1587341 reaction equation
[CH2:1]([O:3][C:4]([N:6]1[CH2:10][CH2:9][C@H:8]([CH2:11][CH2:12][O:13][CH2:14][O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C@@H:7]1[C:23]([O:25][CH2:26][CH3:27])=[O:24])=[O:5])[CH3:2].C([Li])CCC.Cl>C(O)C>[CH2:1]([O:3][C:4]([N:6]1[CH2:10][CH2:9][C@@H:8]([CH2:11][CH2:12][O:13][CH2:14][O:15][CH2:16][C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)[C@@H:7]1[C:23]([O:25][CH2:26][CH3:27])=[O:24])=[O:5])[CH3:2]

Participants

5

Procedure

A solution of 6.2 g of cis ethyl 1-ethoxycarbonyl-3-[2-(benzyloxymethoxy)ethyl]-pyrrolidine-2-carboxylate in 75 ml of anhydrous ethanol containing 1 ml of butyllithium (1.6M) is refluxed under nitrogen for 6 days. After cooling, 1.7 ml of 1N hydrochloric acid is added, the solution is concentrated in vacuo, cold water added and mixture extracted with methylene chloride. The extract is dried over sodium sulfate, filtered, concentrated and purified by high pressure liquid chromatography using ethyl acetate/hexane (15:85) to yield trans ethyl 1-ethoxycarbonyl-3-[2-(benzyloxymethoxy)-ethyl]-pyrrolidine-2-carboxylate.

Workup

  1. temperatureAfter cooling
  2. concentrationthe solution is concentrated in vacuo, cold water
  3. additionadded
  4. extractionmixture extracted with methylene chloride
  5. dry with materialThe extract is dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. custompurified by high pressure liquid chromatography

Sources & evidence

ORD record
ord-d37c578edec84c1da7bc037d9be8af43
Source dataset
uspto-grants-1993_06
Patent number
US05217963

Reaction notes

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