HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643812Generated: October 25, 2026
1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → tert-butyl L-prolinate
https://huagongshe.com/reaction/643812
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 5-[(4-Phenylphenoxy)methyl]furan-2-carboxylic acid | HCID 4683153 | — |
| Reactant | tert-butyl (2R)-pyrrolidine-2-carboxylate hydrochloride | HCID 44629909 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-butyl L-prolinate | HCID 102884 | 61.1% |
Reaction Steps
A solution of 5-(biphenyl-4-yloxymethyl)-furan-2-carboxylic acid (of Intermediate 8; 0.134 g, 0.46 mmol), D-proline tert-butyl ester hydrochloride (Bachem; 0.22 g, 1.1 mmol), 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (Avocado; 0.18 g, 0.95 mmol), and N,N-dimethylaminopyridine (0.166 g, 1.36 mmol) in tetrahydrofuran (10 mL) was stirred at room temperature for 16 h. The solvents were evaporated under reduced pressure, and water and ethyl acetate were added. The aqueous phase was extracted three times with ethyl acetate, and the combined organic layers were dried (sodium sulfate), filtered, evaporated, and purified using a Biotage Flash 40 purification system, eluting with methylene chloride/acetone 9:1, to give 5-(biphenyl-4-yloxymethyl)-furan-2-carbonyl]-D-pyrrolidine-2-carboxylic acid tert-butyl ester as a white solid (0.115 g, 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700632B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-4b55ed77f1a04cefaed8fcc07fbb4178 |
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| Source note | uspto-grants-2010_04 |
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