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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066032Generated: November 2, 2026

(Diethoxyphosphinyl)acetic acid → HCID 86756983, compound

https://huagongshe.com/reaction/1066032

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethoxyphosphinyl)acetic acidHCID 36704—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 13933000HCID 13933000—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86756983HCID 8675698380%

Reaction Steps

A solution of compound 35 (0.360 g, 1.24 mmol), diethylphosphonoacetic acid (0.266 g, 1.36 mmol, prepared as disclosed by M. P. Cooke, K. B. Bicunas, Synthesis, 283, 1981, and 1-hydroxybenzotriazole (0.251 g, 1.86 mmol) in anhydrous THF (15 ml) was treated with 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.285 g, 1.49 mmol). The mixture was stirred at rt for 24 h, and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on 230-400 mesh silica gel (Macherey-Nagel Silica Gel 60 Art. Nr. 81538) eluting with CH2Cl2-hexane-MeOH (98:70:4) and collecting 4 mL fractions. The appropriate fractions were combined, evaporated, and pump-dried to give intermediate 36 (0.464 g, 80%) as an oil: 1H-NMR (CDCl3, 80 Mhz) δ 1.33 (t, 6H, J=7.1 Hz, 2×CH3CH2), 1.60 (s, 9H, 3×CH3), 1.67 (s, 6H, 2×CH3), 2.02 (m, 12H, 6×CH2), 2.83 (d, 2H, J=20 Hz, CH2P), 3.86 (d, 2H, J=7.1 Hz, CH2), 4.14 (q, 4H, J=7.1 Hz, 2×CH3CH2), 5.10 (br, 3H, 3×CH), 5.20 (t, 1H, J=7.1 Hz, CH); MS (FAB+) m/e 468 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242433B1
Source datasetuspto-grants-2001_06
ORD IDord-4bf1968446054dafa3a93cb9281a33c9
Source noteuspto-grants-2001_06