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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849027Generated: November 3, 2026

Hydrochloric Acid → HCID 9949326, compound

https://huagongshe.com/reaction/849027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantDibenzyl 2-methylenepentanedioateHCID 10947302—
ReactantHCID 18403163HCID 18403163—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 9949326HCID 9949326125.1%

Reaction Steps

To a solution of 4-methylbenzyl-O-benzylphosphinic acid (2, R=4-methylbenzyl)(2.16 g, 8.3 mmol) in THF (15 mL) was added sodium hydride (0.10 g, 60% dispersion in oil) followed by dibenzyl 2-methylenepentanedioate at 0 C., and the mixture was stirred at rt for 4 h. The reaction mixture was then diluted with EtOAc (50 mL) and poured into 1N HCl (50 mL). The organic layer was separated, dried over Na2SO4, and concentrated. This material was purified by silica gel chromatography (hexanes:EtOAc, 4:1 to 1:1) to give 3.41 g of 2,4-di(benzyloxycarbonyl)butyl(4-methylbenzyl)-o-benzylphosphinic acid (4, R=4-methylbenzyl) as colorless oil (70% yield): Rf 0.61 (EtOAc); 1H NMR (CDCl3) delta 1.6-1.8 (m, 1H), 1.9-2.0 (m, 2H), 2.1-2.4 (m, 6H), 2.7-2.9 (m, 1H), 3.05 (dd, J=9.0, 16.8 Hz, 2H), 4.8-5.1 (m, 6H), 7.0-7.1 (m, 4H), 7.2-7.4 (m, 15H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06011021
Source datasetuspto-grants-2000_01
ORD IDord-e97e5902c3424df28f82c477cb13c07f
Source noteuspto-grants-2000_01