Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1794251Generated: October 26, 2026

1-Bromo-4-chlorobutane → Ethyl 6-chloro-2-ethoxycarbonyl-2-(p-toluoylamino)hexanoate

https://huagongshe.com/reaction/1794251

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-chlorobutaneHCID 81364—
ReactantSodiumHCID 5360545—
ReactantDiethyl p-toluoylaminomalonateHCID 17447783—
SolventEthanolHCID 702—
ProductEthyl 6-chloro-2-ethoxycarbonyl-2-(p-toluoylamino)hexanoateHCID 2186678154.6%

Reaction Steps

Sodium (6.42 g) was dissolved in 390 ml of ethanol at room temperature. To the solution was added 78.0 g of diethyl p-toluoylaminomalonate, and 47.9 g of 1-bromo-4-chlorobutane was added dropwise under heating to reflux. The mixture was heated to reflux for 20 hours. The reaction solution was concentrated. To the residue was added water, and the mixture was washed with ethyl acetate. After washing with 10% hydrochloric acid and water sequentially, the solution was dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (Wakogel® C-200, n-hexane:ethyl acetate=9:1) to provide 55.7 g of the objective compound as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022723B2
Source datasetuspto-grants-2006_04
ORD IDord-1f8a80d393754effbd1c0054bc3e0d23
Source noteuspto-grants-2006_04