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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 989625Erstellt: 25. Oktober 2026

Water → Di-tert-butyl 2-[[[2-(benzylcarboxy)propyl]tert-butoxyphosphinyl]methyl]pentanedioate

https://huagongshe.com/reaction/989625

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktBenzyl methacrylateHCID 17236—
EduktSodium hydrideHCID 24758—
EduktHCID 178451016HCID 178451016—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktDi-tert-butyl 2-[[[2-(benzylcarboxy)propyl]tert-butoxyphosphinyl]methyl]pentanedioateHCID 1841807453%

Reaktionsschritte

To a solution of di-tert-butyl 2-[(tert-butoxy-phosphinyl)methyl]pentane-l,5-dioate (13.62 g, 36.0 mmol) and benzyl methacrylate (6.35 g, 36.0 mmol) in THF (100 ml) under nitrogen was added sodium hydride (0.14 g, 60% dispersion in oil, 3.60 mmol). After three hours, the reaction mixture was poured into water (300 ml) and ether (100 ml) was added. The organic layer was separated and retained, and the aqueous layer was washed again with ether (100 ml). The combined organic extracts were dried over magnesium sulfate and the solvent was removed under reduced pressure. The resulting residue was purified by column chromatography and the product was eluted with 2:3 EtOAc/Hexane. The solvent was removed under reduced pressure leaving a clear oil (10.5 g, 53%). 1H NMR (CDCl3) : δ 1.3 (m, 3H), 1.5 (m, 27H), 1.7 (m, 2H), 1.9 (m, 2H), 2.2 (m, 4H), 2.6 (m, 1H), 2.9 (m, 1H), 5.1 (m, 2H), 7.3 (m, 5H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06458775B1
Quelldatensatzuspto-grants-2002_10
ORD IDord-35c7d8c9469744a18055546c3631a8ae
Quellennotizuspto-grants-2002_10