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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCinnamaldehydeHCID 637511—
EduktSparteineHCID 644020—
EduktHCID 59094988HCID 59094988—
KatalysatorTitanium TetrachlorideHCID 24193—
LösungsmittelDichloromethaneHCID 6344—
Produkt(4R)-4-Benzyl-3-{(2R,3R)-2-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-3-hydroxy-5-phenyl-pent-4-enoyl}-oxazolidin-2-oneHCID 6974783983,2%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06949546B2
Quelldatensatzuspto-grants-2005_09
ORD IDord-906f29d688e64af9acd4ae62ff716c69
Quellennotizuspto-grants-2005_09