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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745342Generated: October 29, 2026

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

https://huagongshe.com/reaction/745342

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 numberUS04598071
Source datasetuspto-grants-1986_07
ORD IDord-e3fd677cfe884510bbd2b8d94105c887
Source noteuspto-grants-1986_07