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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130563Erstellt: 24. Oktober 2026

Benzyl iodide → HCID 11160280, Verbindung

https://huagongshe.com/de/reaction/130563

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl iodideHCID 12098—
EduktLithium HexamethyldisilazideHCID 2733832—
Edukt(S)-beta-(2-propyl)-gamma-butyrolactoneHCID 11083905—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 11160280HCID 1116028058%

Reaktionsschritte

Lithium bis(trimethylsilyl)amide (1.0 M solution in THF, 92 mL, 92 mmol) was added in 3-5 minutes to a solution of (S)-β-(2-propyl)-γ-butyrolactone 175 (11.68 g, 91.25 mmol) in dry THF 100 mL at −78° C. under argon atmosphere. It was stirred for 1 h and a solution of benzyl iodide (21.87 g, 100.37 mmol )in dry THF was added rapidly. Stirring was continued for 1.5 hours and quenched at −78° C. by the addition of a solution of brine followed by ethyl acetate. The organic phase was separated and the aqueous was further extracted with ether. Chromatography on silica gel first eluted with 5% methylene chloride in pet ether, and finally with 10% ether in pet ether gave desired compound 11.6 g, 58%. NMR (CDCl3) δ 7.19 (m, 5H, C6H5), 4.02 (app. t, 1H, CHaHbO), 3.87 (dd, 1H, CHaHbO), 2.98 (d, 2H, ArCH2), 2.57 (q, 1H, BnCHC═O), 2.05 (m, 1H, CHCH(Me)2, 1.55 (m, 1H, CH(Me)2), 0.81 (d, 3H, CH3) and 0.72 (d, 3H, CH3).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381747B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-0f055982e9ea44dfaa6392f0b6ca3e38
Quellennotizuspto-grants-2008_06