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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1182092Erstellt: 26. Oktober 2026

Imidazole → Benzyl (S)-3-(Boc-amino)-4-iodobutanoate

https://huagongshe.com/reaction/1182092

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktIodineHCID 807—
EduktTriphenylphosphineHCID 11776—
EduktPhenylmethyl (3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutanoateHCID 10040985—
LösungsmittelDichloromethaneHCID 6344—
ProduktBenzyl (S)-3-(Boc-amino)-4-iodobutanoateHCID 11258642—

Reaktionsschritte

A suspension of polymer bound triphenyl phosphine (18.25 g, 54.76 mmol) in DCM (100 ml) is treated with iodine (12.2 g, 48.1 mmol) and the reaction mixture stirred at ambient temperature for 15 minutes. Imidazole (3.72 g, 54.7 mmol) is added and the reaction mixture stirred for a further 15 minutes. A solution of (S)-3-tert-butoxycarbonylamino-4-hydroxy-butyric acid benzyl ester (6.76 g, 21.9 mmol) in DCM (100 ml) is added. The suspension is stirred at reflux for 1.5 hours, then filtered through Celite™ filter material, washing through with DCM. The combined organic phase is washed with an aqueous solution of 10% sodium thiosulphate, water and brine, then dried over magnesium sulphate and evaporated. The crude product is chromatographed over flash silica using 8% ethylacetate in iso-hexane as eluent to afford (S)-3-tert-butoxycarbonylamino-4-iodo-butyric acid benzyl ester. [M-BOC] 320.12

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07288537B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-03e7a4abcdd845eca11b0eb3e0bc38af
Quellennotizuspto-grants-2007_10