Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837922Generated: October 25, 2026

Propionic Acid → 3-(Quinolin-3-yl)-hex-4-enoic acid ethyl ester

https://huagongshe.com/reaction/1837922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionic AcidHCID 1032—
ReactantTriethyl orthoacetateHCID 66221—
Reactant4-(Quinolin-3-yl)-but-3-en-2-olHCID 54229904—
SolventSodium chloride; waterHCID 57417360—
Product3-(Quinolin-3-yl)-hex-4-enoic acid ethyl esterHCID 54155846—

Reaction Steps

A solution of the allylic alcohol 22-2 (1.2 g, 6.1 mmol) in triethyl orthoacetate (50 mL) was treated with propionic acid (0.022 mL, 0.31 mmol) and refluxed for 2 h. The cooled mixture was treated with a solution of 1:1 sat. brine/1N HCl (150 mL), then extracted with CH2Cl2 (3×125 mL). The pooled organic extracts were washed with sat. NaHCO3, dried, filtered and evaporated. Chromatography on silica gel (EtOAc) afforded 22-3 as a yellow glass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784190B2
Source datasetuspto-grants-2004_08
ORD IDord-8bc253619949475d91a0e7848cf74503
Source noteuspto-grants-2004_08