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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072965Generated: October 26, 2026

Methionin AL → 6-(3,5-Dimethylbenzyl)-5-isopropyluracil

https://huagongshe.com/reaction/1072965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethionin ALHCID 446793—
ReactantThioureaHCID 2723790—
ReactantEthyl 3-methyl-2-(3,5-dimethylphenylacetyl)butanoateHCID 21635576—
SolventEthanolHCID 702—
Product6-(3,5-Dimethylbenzyl)-5-isopropyluracilHCID 1073090154%

Reaction Steps

Metal sodium (23.8 g, 1.034 mol) was reacted with anhydrous ethanol (500 ml). To the clear obtained solution, was added thiourea (54.35 g, 714 mmol) and ethyl 3-methyl-2(3,5-dimethylphenylacetyl)butanoate (13.14 g, 47.6 mol). The reaction medium was maintained under reflux for 6 h, and then was concentrated in vacuo at 40.50° C. To the obtained residue was added concentrated hydrochloric acid (100 ml) and then the solution was brought to pH 4 with acetic acid. The obtained 6-dimethylbenzyl-5-isopropyl-2-thiouracil was dissolved in an aqueous 10% chloroacetic acid solution (200 ml) and the solution was maintained under reflux for 24 h and then cooled to ambient temperature and the obtained precipitates were separated by filtration and washed with cold ethanol and then with ether, and then dried in vacuo at 40° C. to give 6-(3,5-dimethylbenzyl)-5-isopropyluracil (7 g, 54%). Melting point: 213-214° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911450B1
Source datasetuspto-grants-2005_06
ORD IDord-cb0ad1968cf54acca043b32b31b7d52f
Source noteuspto-grants-2005_06