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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388694Generated: October 28, 2026

Triethylamine → HCID 131713398, compound

https://huagongshe.com/reaction/1388694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantDiethyl 4-phenylbutylphosphonateHCID 13102400—
ReactantHCID 131713399HCID 131713399—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131713398HCID 131713398—

Reaction Steps

A mixture of (4-phenylbutyl)phosphonic acid, diethyl ester (0.97 g., 3.6 mmole), dry benzene (10 ml.), and phosphorus pentachloride (0.75 g., 3.6 mmole) is refluxed under argon for 20 minutes. The phosphorus oxychloride and benzene are removed in vacuo, and the residue is taken up in dry tetrahydrofuran (10 ml.) and treated with N-(L-alanyl)-N-methylglycine, ethyl ester, hydrochloride (0.67 g., 3.0 mmole). The resulting suspension is cooled to 0° (ice-bath) and treated dropwise with triethylamine (1.2 ml., 3.0 eq.) in tetrahydrofuran (5 ml.) over a period of 2 minutes in an argon atmosphere. After stirring at 0° for 20 minutes the ice bath is removed and the reaction mixture is stirred for an additional 4 hours. The reaction mixture is then diluted with ethyl acetate and washed successively with 5% potassium bisulfate, saturated sodium bicarbonate, brine, dried (MgSO4), and evaporated. The residue (1.4 g.) is chromatographed on silica gel (60 g.) eluting with toluene/acetone (1:1) to give 1.0 g. of N-[N-[ethoxy(4-phenylbutyl)phosphinyl]-L-alanyl]-N-methylglycine, ethyl ester as an oil after evaporation. Tlc (toluene/acetone; 1:1) shows a single spot at Rf =0.19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04432972
Source datasetuspto-grants-1984_02
ORD IDord-1387a3a5d0e04a20a9f8d2645cd26261
Source noteuspto-grants-1984_02