HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 497479Erstellt: 25. Oktober 2026
Cinnamaldehyde → (4R)-4-Benzyl-3-{(2R,3R)-2-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-3-hydroxy-5-phenyl-pent-4-enoyl}-oxazolidin-2-one
https://huagongshe.com/reaction/497479
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Cinnamaldehyde | HCID 637511 | — |
| Edukt | Sparteine | HCID 644020 | — |
| Edukt | HCID 59094988 | HCID 59094988 | — |
| Katalysator | Titanium Tetrachloride | HCID 24193 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (4R)-4-Benzyl-3-{(2R,3R)-2-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-3-hydroxy-5-phenyl-pent-4-enoyl}-oxazolidin-2-one | HCID 69747839 | 83,2% |
Reaktionsschritte
To a stirring solution of (R)-4-benzyl-3-[5-(tert-butyl-diphenyl-silanyloxy)-pentanoyl]-oxazolidin-2-one (1.64 g, 3.19 mmol) in dry methylene chloride (15.9 mL) in a flame dried round bottom flask under N2 at 0° C. was added titanium(IV) chloride (386 μL, 3.51 mmol). After 5 min, (−)-sparteine (1.83 mL, 7.97 mmol) was added. After 20 min, trans-cinnamaldehyde (442 μL, 3.51 mmol) was added dropwise to the purple suspension, and the resulting pale green-yellow solution was stirred for 1 h. The reaction was quenched by the addition of 50% saturated ammonium chloride (50 mL), diluted with water (100 mL), and then extracted with methylene chloride (3×30 mL). The organic layers were combined, washed with brine, dried over sodium sulfate, and concentrated in vacuo to a colorless oil. The oil was purified by flash chromatography (SiO2, 15-30% ethyl acetate in hexanes) to yield 1.72 g (83.1%) of the desired product as a white solid. MS (APCI), m+/z: (M+H)+=648.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06949546B2 |
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| Quelldatensatz | uspto-grants-2005_09 |
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| ORD ID | ord-906f29d688e64af9acd4ae62ff716c69 |
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| Quellennotiz | uspto-grants-2005_09 |
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