HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → trans-3-Ethyl-DL-proline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Diethyl 3-ethyl-1,3-dihydro-2H-pyrrole-2,2-dicarboxylate | HCID 21866300 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | trans-3-Ethyl-DL-proline | HCID 10154109 | 75.6% |
Reaction Steps
The pyrroline (4.68 g, 19.5 mM) was added to a mixture of 1M NaOH (80 ml) and ethanol (80 ml) and the solution stirred at 50° for 4 hrs. The solution was then cooled, sodium borohydride (1.0 g) added, and stirred at 25° for a further 10 hours. The solution was then carefully acidified with dilute HCl to pH 4, concentrated and applied to a column of Dowex 50WX8 resin (H+ form, 100 ml) Elution with aqueous ammonia (2 M) yielded a solution which on evaporation gave trans-3-ethyl-dl-proline (2.1 g) m.p. 208≈-209°; RF 3B 0.43. Analysis on a Jeol 6AH amino acid analyser (50 cm column, sodium citrate buffer 0.2 N, pH 3.25 temperature 57°) showed a single peak (elution time 117 mins).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04060603 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-78139d2248db4102a824ac78fd8f37ad |
| Source note | uspto-grants-1977_11 |