Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | methyl L-prolinate hydrochloride | HCID 2733200 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Methyl L-prolinate | HCID 853477 | 119,1% |
Reaktionsschritte
To a solution of L-proline methyl ester hydrochloride (257 mg, 1.43 mmol) in MeOH was added triethylamine (0.2 mL, 1.43 mmol). The solution was concentrated under reduced pressure to give a white solid residue, which was triturated with ether (3×). The collected ether solution was concentrated under reduced pressure to give L-proline methyl ester free amine (220 mg) as a colorless oil. To a solution of above free amine in toluene (5 mL) was added compound 1A (278 mg, 1.3 mmol), followed by 4 Å molecular sieves (1.0 g). The mixture was stirred at room temperature overnight and filtered. The filtrate was diluted with EtOAc, washed with 1 N aqueous HCl, water, brine, dried over MgSO4, concentrated under reduced pressure to give a crude product, which was chromatographed (silica gel) eluting with CH2Cl2, 0.5% MeOH in CH2Cl2 to give the title compound (410 mg, 92% yield) as a yellow foam.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06670386B2 |
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| Quelldatensatz | uspto-grants-2003_12 |
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| ORD ID | ord-16d4886752374489ac6f02c5481ed97c |
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| Quellennotiz | uspto-grants-2003_12 |
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