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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954035Generated: November 2, 2026

Quinoline → HCID 23296051, compound

https://huagongshe.com/reaction/1954035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinolineHCID 7047—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 23296057HCID 23296057—
ProductHCID 23296051HCID 23296051—

Reaction Conditions

Temperature185 °C

Reaction Steps

20 g of methyl 4-methoxy-3-(2-methyl-2-propenyloxy)benzoate are dissolved in 60 ml of quinoline and the mixture is heated at 180-190° C. for 2 h. After cooling, it is treated with ethyl acetate and the quinoline is extracted using 2N HCl. The organic phase is washed a further 2 times with water and concentrated. The oily residue is chromatographed on a silica gel column using ethyl acetate/petroleum ether (4:6). The chromatographically pure fractions are combined, concentrated and dried in a high vacuum. 15.6 g of the title compound are obtained as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06121274
Source datasetuspto-grants-2000_09
ORD IDord-e9f9b6f73970403db1776cf9970662d2
Source noteuspto-grants-2000_09