Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 553280Erstellt: 24. Oktober 2026

Tri-o-tolylphosphine → Tert-butyl 2,6-dichlorophenethyl(3-(2-oxopropyl)benzyl)carbamate

https://huagongshe.com/de/reaction/553280

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTri-o-tolylphosphineHCID 80271—
EduktMethoxytri-n-butylstannaneHCID 11964040—
Edukt1-Acetoxy-3-methyl-1,3-butadieneHCID 53401854—
Edukt[2-(2,6-Dichloro-phenyl)-ethyl]-(3-iodo-benzyl)-carbamic acid tert-butyl esterHCID 67165818—
LösungsmittelTolueneHCID 1140—
ProduktTert-butyl 2,6-dichlorophenethyl(3-(2-oxopropyl)benzyl)carbamateHCID 67165764—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

[2-(2,6-Dichloro-phenyl)-ethyl]-(3-iodo-benzyl)-carbamic acid tert-butyl ester (Example 14, step b) (500 mg), tributyltin methoxide (350 μL), isoprenyl acetate (170 μL), tri-o-tolylphosphine (30 mg) and toluene (20 mL) were charged to a flask and the solution degassed with nitrogen for 5 minutes. Palladium acetate (10 mg) was added and the resultant mixture heated to 100° C., under nitrogen, for 3 hours. On cooling, potassium fluoride (580 mg) in water (3 mL) was added, stir at room temperature for 18 hours. The solids were filtered off, and the filter cake washed with ethyl acetate. The filtrate was evaporated and purified on silica, eluting with a gradient of iso-hexane/ethyl acetate [4:1 to 2:1], to give the subtitle product as an oil (230 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07951954B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-ad8f92d1c2294bb6a3c2dd8618b77800
Quellennotizuspto-grants-2011_05