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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989625Generated: October 25, 2026

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

https://huagongshe.com/reaction/989625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl methacrylateHCID 17236—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178451016HCID 178451016—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductDi-tert-butyl 2-[[[2-(benzylcarboxy)propyl]tert-butoxyphosphinyl]methyl]pentanedioateHCID 1841807453%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458775B1
Source datasetuspto-grants-2002_10
ORD IDord-35c7d8c9469744a18055546c3631a8ae
Source noteuspto-grants-2002_10