Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | D-Proline | HCID 8988 | — |
| Edukt | 1,2-Bis(phenylmethyl) 1,2-diazenedicarboxylate | HCID 75557 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 3-(Oxan-4-yl)propanal | HCID 57449683 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | HCID 57786523 | HCID 57786523 | 89% |
Reaktionsschritte
To a stirred solution of 3-(tetrahydro-pyran-4-yl)-propionaldehyde (8.59 g, 0.06 mol) and dibenzyl azodicarboxylate (12.8 g, 0.042 mol) in MeCN (250 mL) at 0° C. was added (R-proline) (0.48 g, 0.0042 mol). After stirring the mixture at 0° C. for 15 h, ethanol (100 mL) and NaBH4 (1.56 g, 0.042 mol) were added, and the mixture was stirred at 0° C. for 40 min. The reaction was quenched by slow addition of 10% aq citric acid (15 mL), and the whole solution was concentrated in vacuo. This residue was diluted with EtOAc (200 mL), washed with brine (50 mL), dried over Na2SO4, and concentrated in vacuo to give crude product which was purified by column chromatography to give (S)-dibenzyl 1-(1-hydroxy-3-(tetrahydro-2H-pyran-4-yl)propan-2-yl)hydrazine-1,2-dicarboxylate (16.52 g, 89%). 1H NMR (CD3OD) δ 1.0-1.5 (m, 8H), 2.9-3.3 (m, 2H), 3.4-3.6 (m, 2H), 3.7-3.9 (m, 2H), 4.4-4.7 (m, 2H), 5.1-5.4 (m, 4H), 7.2-7.4 (m, 10H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07872028B2 |
|---|
| Quelldatensatz | uspto-grants-2011_01 |
|---|
| ORD ID | ord-e081292ec63447d6af8e1dcf1288bce3 |
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| Quellennotiz | uspto-grants-2011_01 |
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