HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 396724Erstellt: 23. Oktober 2026
(S)-(-)-N-Benzyl-1-phenylethylamine → methyl 3-{R}-[benzyl-({S}-1-phenyl-ethyl)-amino]-3-(1-boc-1,2,3,4-tetrahydro-quinolin-6-yl)-propionate
https://huagongshe.com/de/reaction/396724
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | (S)-(-)-N-Benzyl-1-phenylethylamine | HCID 1268085 | — |
| Edukt | Methyl 3-(1-boc-1,2,3,4-tetrahydro-quinolin-6-yl)acrylate | HCID 54398523 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | methyl 3-{R}-[benzyl-({S}-1-phenyl-ethyl)-amino]-3-(1-boc-1,2,3,4-tetrahydro-quinolin-6-yl)-propionate | HCID 21354704 | — |
Reaktionsschritte
A solution of (S)-N-benzyl-α-methylbenzylamine (2.6 ml) in anhydrous tetrahydrofuran (50 ml), cooled to −70° C. and under nitrogen, was treated dropwise with a solution of butyllithium in hexanes (5 ml, 2.5M) over about 5 minutes to give a red solution. After stirring at −70° C. for a further 40 minutes the mixture was treated dropwise with a solution of methyl 3-(1-boc-1,2,3,4-tetrahydro-quinolin-6-yl)acrylate [2.0 g, Reference Example 7(d)] in tetrahydrofuran (20 ml) over about 10 minutes. Stirring was continued at low temperature for a further 20 minutes and then the reaction mixture was allowed to warm to room temperature. The mixture was partitioned between ether and water, the layers separated, and the organic layer washed with water then with brine, then dried and then evaporated. The residue was subjected to flash chromatography on silica eluting with a mixture of ethyl acetate and petrol (initially 1:9 and then 15:85, v/v) to give the title compound as a viscous, colourless oil, 1.5 g.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06608084B1 |
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| Quelldatensatz | uspto-grants-2003_08 |
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| ORD ID | ord-f504505246fc43f2b89bbd34262b5278 |
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| Quellennotiz | uspto-grants-2003_08 |
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