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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484760Generated: October 30, 2026

Triethylamine → (S)-Hexahydro-3-[[ethoxy(4-phenylbutyl)phosphinyl]amino]-2-oxo-1H-azepine-1-acetic acid, ethyl ester

https://huagongshe.com/reaction/484760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthoxy(4-phenylbutyl)phosphinyl chlorideHCID 15591238—
Reactant3-amino-2-oxo-hexahydro-1H-azepine-1-acetic acid, ethyl ester, monohydrochlorideHCID 131714292—
SolventTetrahydrofuranHCID 8028—
Product(S)-Hexahydro-3-[[ethoxy(4-phenylbutyl)phosphinyl]amino]-2-oxo-1H-azepine-1-acetic acid, ethyl esterHCID 86740216—

Reaction Steps

A mixture of ethoxy(4-phenylbutyl)phosphinyl chloride [4.4 mmole; prepared as set forth in Example 1(f)], dry tetrahydrofuran (10 ml.), and 3-amino-2-oxo-hexahydro-1H-azepine-1-acetic acid, ethyl ester, monohydrochloride (1.0 g., 4.0 mmole) at 0° (ice bath) in an argon atmosphere is treated dropwise with triethylamine (1.7 ml., 3.0 eq.) in tetrahydrofuran (5 ml.) over 2 minutes. After 20 minutes, the ice bath is removed and the reaction mixture is stirred for an additional 1.5 hours. The reaction mixture is diluted with ethyl acetate and washed successively with saturated sodium bicarbonate, 5% potassium bisulfate, and brine, dried (MgSO4) and evaporated. The residue (2.1 g.) is chromatographed on silica (65 g.) eluting with ethyl acetate then acetone to give 1.0 g. of (S)-hexahydro-3-[[ethoxy(4-phenylbutyl)phosphinyl]amino]-2-oxo-1H-azepine-1-acetic acid, ethyl ester as an oil after evaporation. TLC (ethyl acetate) single spot at Rf =0.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04533661
Source datasetuspto-grants-1985_08
ORD IDord-14580fba7e4d474ba4b918e496e78478
Source noteuspto-grants-1985_08