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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196043Generated: November 2, 2026

Triethylamine → N-(3-ethoxycarbonylpropyl)-N-[2-(chroman-3-yl)ethyl]-amine

https://huagongshe.com/reaction/1196043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 4-bromobutyrateHCID 76300—
Reactant2-(3,4-dihydro-2H-1-benzopyran-3-yl)ethan-1-amineHCID 14838408—
SolventMethanolHCID 887—
ProductN-(3-ethoxycarbonylpropyl)-N-[2-(chroman-3-yl)ethyl]-amineHCID 14838465—

Reaction Steps

17.7 g (0.1 mol) of 3-(2-aminoethyl)chroman are dissolved in 100 ml of methanol, and then 10.5 g (0.1 mol) of triethylamine and 19.5 g (0.1 mol) of 4-bromobutyric acid ethyl ester are added to the solution. The reaction mixture is stirred for 15 hours at room temperature and is then concentrated under a water-jet vacuum. The residue is taken up in diethyl ether and washed neutral with ice-water. The ethereal phase is dried over potassium carbonate and concentrated by evaporation. Oily N-(3-ethoxycarbonylpropyl)-N-[2-(chroman-3-yl)ethyl]-amine is thus obtained and can be used further in crude form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112855
Source datasetuspto-grants-1992_05
ORD IDord-6c382037d0704bc1bbecabd86769aec6
Source noteuspto-grants-1992_05