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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818656Generated: October 28, 2026

Toluene → 3-(4-chloro-phenoxy)-N-[2-(3-methoxy-4-prop-2-ynyloxy-phenyl)-ethyl]-2-prop-2-ynyloxy-propionamide

https://huagongshe.com/reaction/1818656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPropargyl bromideHCID 7842—
ReactantSodium HydroxideHCID 14798—
Reactant3-(4-chloro-phenoxy)-2-hydroxy-N-[2-(3-methoxy-4-prop-2-ynyloxyphenyl)-ethyl]-propionamideHCID 11750051—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
Product3-(4-chloro-phenoxy)-N-[2-(3-methoxy-4-prop-2-ynyloxy-phenyl)-ethyl]-2-prop-2-ynyloxy-propionamideHCID 44453952—

Reaction Steps

A 80% solution of propargyl bromide in toluene (1.6 g, 11 mmol) is added slowly at room temperature to a mixture of 3-(4-chloro-phenoxy)-2-hydroxy-N-[2-(3-methoxy-4-prop-2-ynyloxy-phenyl)-ethyl]-propionamide (3.5 g, 8.7 mmol), 30% sodium hydroxide solution (4.5 ml, 44 mmol) and catalytic amounts of tetrabutylammonium bromide (50 mg) in 30 ml of dichloromethane. The reaction is stirred for 16 hours at +40° C. Subsequently the mixture is evaporated and the residue is diluted with water and dichloromethane. The phases are separated and the aqueous phase is extracted three times with dichloromethane. The combined organic layer is washed with brine, dried over sodium sulfate and evaporated. The remaining oil is purified by chromatography on silica gel (ethyl acetate/hexane 1:1) to yield 3-(4-chloro-phenoxy)-N-[2-(3-methoxy-4-prop-2-ynyloxy-phenyl)-ethyl]-2-prop-2-ynyloxy-propionamide (Compound E1.24).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601674B2
Source datasetuspto-grants-2009_10
ORD IDord-53d754341a684dc680f3ccc42bb9b4e0
Source noteuspto-grants-2009_10