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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377177Generated: October 31, 2026

Hydrochloric Acid → HCID 9903422, compound

https://huagongshe.com/reaction/377177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantDibenzyl 2-methylenepentanedioateHCID 10947302—
ReactantHCID 18403163HCID 18403163—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 9903422HCID 9903422154.3%

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, dired 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, 1 H), 1.9-2.0 (m, 2 H), 2.1-2.4 (m, 6 H), 2.7-2.9 (m, 1 H), 3.05 (dd, J=9.0, 16.8 Hz, 2 H), 4.8-5.1 (m, 6 H), 7.0-7.1 (m, 4 H), 7.2-7.4 (m, 15 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06025344
Source datasetuspto-grants-2000_02
ORD IDord-9a139e73ecb44ccaa8137f30fae7d2e4
Source noteuspto-grants-2000_02